craigslist | science/biotech jobs in los angeles

Research Coordinator/Clinical Data Manager (Arcadia, CA)

2009-11-10T13:32:06-08:00

CURESEARCH NATIONAL CHILDHOOD CANCER FOUNDATION is dedicated to raising private funds for childhood cancer research for the Children's Oncology Group (COG), the world's largest cooperative cancer research organization. Together, we are committed to conquering childhood cancer through scientific discovery and compassionate care. The COG is a network of more than 5,000 physicians, nurses, and scientists whose collaboration, research and care have turned childhood cancer from a virtually incurable disease to one with an overall 78% cure rate.

In addition to a meaningful cause and professional work environment, we offer excellent benefits (medical, dental, vision, 403B with match, gym membership) and promote work-life balance. For more information, please visit: www.curesearch.org.

We are currently seeking a RESEARCH COORDINATOR (aka Clinical Data Manager) for our Phase I Consortium. The RC is responsible for managing all aspects of study coordination and data acquisition for a group of COG studies. This entails coordination of data collection from institutional investigators, laboratory researchers and study committee members as well as preparation of ad-hoc reports as needed. The RC of a COG study will be the primary contact for that study between the Data Center and COG institutional participants in the study, members of the study committee, the Statistics Department, the Study Development Office (SDO), other COG administrative offices, the Information Technology (IT) Department, and the clinical, laboratory, and resource center staff responsible for performing COG studies. The position will be an RC I or RC II, depending on experience.

RESPONSIBILITIES AND DUTIES:

The responsibilities of the Research Coordinator II include, but are not limited to:

1. Typically maintain a greater study volume than a RC I for both studies in development and studies which are ongoing.
2. Participate in presentations/discussions regarding a disease area of interest for the CRA discipline committee at COG annual Group meetings.
3. Must be fully proficient with all RC related applications (i.e. Study Manager, SDE, RDMS, BRV, etc.)
4. Expected to work with minimal supervision for the majority of their routine responsibilities.

And the all RC I responsibilities and duties listed below:

1. Review sections of study protocols related to patient treatment, supportive care, specimen submission, patient follow-up, and any other sections requiring understanding of clinical or laboratory aspects of COG studies.
2. In collaboration with the study statistician and study committee, design the draft Case Report Forms (CRFs) and data validations required to collect the necessary research data for COG studies.
3. Create new group data elements (GDEs) as needed to capture essential research data for the study, or identify required GDEs from the existing GDE database, following established guidelines and procedures.
4. Based on finalized CRFs, implement data elements and data validations for the Enhanced Remote Data Entry System (eRDES) through the Study Manager application. Complete testing, refinement, documentation and release of these screens adhering strictly to the established development procedures.
5. Manage the conduct of studies including, but not limited to, monitoring patient enrollments and randomizations and closing or suspending studies as determined by protocol design or Study Chair to ensure patient safety. Create and execute the Study Data Review Plan according to established procedures.
6. Monitor the quality of submitted research data through the eRDES reporting module to evaluate timeliness of institutional data submissions and the completeness and internal consistency of data. When necessary, modify or enhance data validations to prevent and correct data errors and omissions that have been identified.
7. Set up and monitor systems for rapid tracking and reporting of dose-limiting toxicities, toxic deaths, severe adverse events (SAEs), treatment failures, or other critical study endpoints, as appropriate for the study.
8. Organize, coordinate, or monitor surgery, chemotherapy, pathology, radiology, and radiation therapy reviews, and accumulate the data from these reviews as determined by the protocol.
9. Work with IT staff to address technical problems or system enhancements affecting data systems.

POSITION REQUIREMENTS:

� Bachelor�s degree or higher in a science-related field or equivalent relevant experience.
� Certification as a Clinical Data Manager (CDM). CCDM or other reputable industry certification for clinical data management.
� Minimum two to three years experience as a CRA, CDM or equivalent combination of experience and education credits or must be a Level I RC for at least 2.
� Experience as a CRA/CDM in a comprehensive cancer center, cooperative group or the pharmaceutical/biotechnology industry is highly desirable.
� High level of basic scripting (SQL) and familiarity with data reporting tools desirable.
� High level of PC literacy is required, including intermediate to advanced knowledge of Microsoft Office software such as MS Word, Excel and Access.
� Excellent written and oral communication skills are essential.
� Critical thinking and reasoning.

Scientific Writer / Protocol Coordinator (Arcadia, CA)

2009-11-10T13:25:53-08:00

Formulation Chemist (Santa Fe Springs)

2009-11-10T11:21:00-08:00

Vitamin and Nutraceutical Manufacturer and Packager seeks Formulation Chemist...

Individual will identify innovative product opportunities; develop formulations, prototypes for customer testing;
design and conduct experiments necessary for development; coordinate and support pilot and factory trials;
carry out stability testing to ensure product shelf life and stability,
and develop and communicate project plans and timelines.

Main Responsibilities:

� Develop solid dose formulations�Chewables, Effervescent, Quick dissolve and Conventional tablets, Capsules.
� Present data and communicate with Nutraceutical customers.
� Provide leadership in executing customer projects�internally and/or outsourced.
� Interpret analytical data and prepare scientific reports.
� Assist in testing, scaling up/validation of new products to commercial scale.
� Provide technical service to customers and distributors.
� Communicate with vendors or excipients and test effects of various excipients.
� Test blending, blending uniformity and unit dosage blend testing.

Specific Job Duties:

� Formulate Design of Experiments and Tests for product performance.
� Assist in the development of solid dose formulation in the chewable, gum, effervescent, quick dissolve and conventional formats.
� Provide technical support/problem solving to customers on existing and new products.
� Working with sales and marketing visit customers to present tech. data /promote product performance.
� Understand/interpret customer requirements.
� Support new product scale up and validation in manufacturing.
� Based on priorities set, manage/coordinate customers� project activities.
� Work with analytical, mfg., quality and sales functions as appropriate.
� Test and provide data on physical and chemical properties of active ingredients and excipients and their interaction in oral dosage forms.
� Conduct and record physico-chemical testing of ingredients and blends, such as, NIR, density, moisture content, compressibility, pH, viscosity, specific gravity, color smell and compare it to the standard, etc.
� Evaluate physical parameters like particle size, granulation, direct compressibility, flow.
� Calculate, test and formulate tablet and capsule coating procedures including polymeric choice, disintegration, dissolution, solubility, uniformity and thickness of coating, etc.
� Calculate and prepare product batch records including yields, loss, and process improvement.
� Support for regulatory compliance of weighing, blending and dosage form production standard operating procedures (SOP) and current Good Manufacturing practices.
� Pilot batch process evaluation.
� Test every lot of every raw material that will be used in final production to make sure that specifications meet what the manufacturers say they are and are the same as previous lost of that material.
� Evaluate test results of product stability, purity and compliance to label claim.

Skill sets required:

� MS Chemist or Pharmacist with leadership qualities; should be self-starter wit initiative.
� Experience in developing Nutraceutical/Pharmaceutical/OTC dosage formulations. A strong understanding of powder and tableting/encapsulation technology is necessary. Strong communication skill is important.
� Neet to have a broad understanding of nutraceutical formulations and processes with a strong experience in problem solving techniques. Computer literacy is a must.
� Prior knowledge of Nutraceuticals a must. Must have demonstrated ability to learn product chemistries quickly.
� Ability to undersnaand interpret customer requirements and translate them into clear product development goals. Should be results-oriented.
� Good team player�Ability to coordinate/push for answers within the internal functional groups (i.e. production, finance, quality, marketing, sales, etc.).
� Analytical knowledge is desireable.
� Supervisory experience (set objectives, review performance, resolve conflicts) with QA/QC Techs will be a PLUS.
� Eligible to work legally in US.

Issues keeping your job? (Los Angeles)

2009-11-10T11:18:39-08:00

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Candidates must be available for a 5-day shoot in the Los Angeles area sometime during the month of January 2010.

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Biomedical literature search (part-time/contract) (UCLA)

2009-11-10T08:02:59-08:00

Need a researcher to perform thorough literature searches in the field of nutrition as it relates to various diseases and physiological states. The typical search query would be something like "how does pyridoxine intake affect omega-3 fatty acid metabolism?". This would translate to numerous MEDLINE searches, retrieving the articles, and organizing/summarizing them.

A lot of this job has to be done at the UCLA campus in order to access various library resources, so it is helpful to live and/or study and/or work on campus or nearby.

The ideal candidate would be a pre-medical student at UCLA, or a recent graduate, or possibly someone studying to be a dietitian or nutritionist. It is very helpful to be interested in the field of nutrition and/or orthomolecular medicine. You will definitely learn a lot about that field as part of the job. It is possible that we will write one or more journal papers, in which case you can be a co-author.

This is a contract job, part-time (very flexible about how much time each week, but roughly 5-10 hours +/-). This is entirely a telecommuting job, pick your own hours.

Please reply by email with your educational or work background.

Chemical Manufacturing Technicians (Torrance)

2009-11-09T14:22:26-08:00

COMPANY
Founded in 1982, Phenomenex has established itself as a leader in separation sciences, dedicated to the development, manufacture and supply of analytical products. Our wide array of High Performance Liquid and Gas Chromatography (HPLC and GC) and Solid Phase Extraction (SPE) products are offered throughout the world from our headquarters in the U.S., wholly-owned subsidiaries, and our extensive international network of partners and distributors.

DUTIES
*Carry out processing steps in a batch manufacturing environment.
*Works on assignments that are moderately complex in nature and in which judgement is required in resolving problems and making routine recommendations.
*Performs manufacturing and/or assembly of chromatographic media and/or components.
*Operates production equipments.
*Weighs,measures and checks raw material to assure batches manufactured contain proper ingredients and quantities.
*Maintain records and work area to comply with SOP�s, company policies and in accordance with GMP/ISO 9000 standards.
* Performs other job-related duties as requested.

KNOWLEDGE, SKILLS AND EXPERIENCE
� Associates Degree or Other Certification in Chemistry preferred.
� At least 2 years of experience in Chemical batch processing
� Ensures all work is accurate and free of errors / defects
� Attention to detail, pay specific attention to tasks
� Sound judgement and reasoning
� Able to perform basic mathematical equations and formuals
� Strong organizational skill, plans and assigns resources in a detailed fashion
� At least 2 years of experience in Chemical batch processing

Polymer Chemist (Los Angeles, CA)

2009-11-09T14:10:29-08:00

Are you an experienced Polymer Chemist? We are looking for a PhD Polymer Chemist to join our team in Los Angeles.

We are seeking a chemist with training and experience in polymer chemistry and polymer synthesis. The successful applicant will be responsible for the development of synthesis procedures in the area of polymer science with a particular focus on scale-up and commercialization of innovative polymers, monomers and reagents.

Required Knowledge/Skills/Abilities:
- Ph.D. in synthetic polymer or organic chemistry.
- 5 years of relevant industrial experience.
- Expertise in UV curable technology.
- Experience in modern polymerization techniques is highly desirable.
- Innovative, hands-on, self-starter, goal-oriented individual with drive for solving problems and finding solutions in a timely manner.
- Project management skills.
- Excellent communication skills.
- Detail-oriented and data driven.

Desirable Knowledge/Skills/Abilities:
- Works safely in the laboratory or plant setting.
- Willing to travel as needed.
- Working knowledge of polymer synthesis and characterization.

**LOCAL APPLICANTS ONLY � MUST LIVE WITHIN DRIVING DISTANCE TO LOS ANGELES**

PLEASE SUMBIT BOTH YOUR RESUME AND SALARY HISTORY

Scientific/Research & Development (Los Angeles)

2009-11-09T12:44:28-08:00

Scientific/ R&D for Nutritional Product Company needed immediately. Must have a PHD in nutrition, bio-chemistry or related field
and have at least 2 years in dietary supplement, nutrition, nutraceutical or pharmaceutical industry. Your job will be to educate consumers
on nutritional products, review and summarize scientific data for product development, work in conjuction with the sales force to disseminate
product information to retailers and support marketing with technical information. You will also draft protocols of clinical and scientific studies.
Must be proficient in all Microsoft programs and know Visio and Outlook. This is a direct hire position and pays 75k/year. Please email your
resume to marciaa@firstcallstaff.com for immediate consideration.

Principle Scientist (Philadelphia, PA)

2009-11-07T12:30:16-08:00

Company Info:

Invisible Sentinel is a recently established biotech company focused on developing and commercializing novel diagnostic products for the specific detection of pathogenic bacteria. Invisible Sentinel�s scientific team will integrate existing technologies with innovative and advanced biomedical engineering methods to achieve our objectives. Invisible Sentinel prides itself on not restricting the limits of the career opportunities that employees can pursue as the company realizes its goal of becoming a global diagnostic biotechnology leader. Invisible Sentinel encourages both the professional and personal growth of our employees and is committed to supplying our employees with the resources they need to realize their full potential.

Job Description:

Invisible Sentinel is seeking a talented and highly motivated biomedical scientist with a strong educational and technical background in the fields of bacteriology and immunology. The successful candidate will need to be familiar with the development and characterization of monoclonal antibodies. This position provides the opportunity to be a member of the core design team and as such you will need to demonstrate high levels of enthusiasm, dedication, and innovation. The core responsibility for this position would be the design and development of assays to characterize monoclonal antibodies specific for various bacterial pathogens.

Responsibilities: Will include (but are not limited to) the following:

Establish and Supervise the antibody design and engineering group.
Expression, purification and characterization of monoclonal antibodies.
Represent antibody expertise in project team meetings and provide flexible support to
colleagues working on correlating company projects.
Manage lab resources and assess performance of team members.

Requirements:

Ph.D. in biological sciences with a minimum of 2 to 3 years practice in protein purification
& monoclonal antibody development.
Strong background and expertise in molecular biology, bacteriology and/or immunology.
Experience with expression, purification, and characterization of monoclonal antibodies is required.
Proven track record and in-depth knowledge of current antibody engineering literature and
characterization protocols.
Team-oriented and pro-active attitude; ability to communicate and interact effectively with management as well
as lab personnel.
Constructively contribute to decision-making and optimization of assay design.

Per Diem Laboratory Technician (Glendale, CA)

2009-11-06T16:44:33-08:00

California Clinical Trials, a subsidiary of PAREXEL International, is searching for a Lab Technician who would like to be a part of a great research team.

Essential Function: The Lab Technician performs all duties related conducting study protocol laboratory procedures for the Early Drug Phase, Phase II-IV, and Sleep Departments.

Key Accountabilities: Including but not limited to the following and other duties as may be assigned:

� Possesses detailed knowledge of study protocol lab procedures.
� Collects, processes and ships safety labs, pharmacokinetic (PK), pharmacodynamic (PD) samples according to clinical study protocol.
� Takes responsibility for 24-hour urine collection and set-up based on our COGs or protocol.
� Take responsibility for lab set-up and supplies (i.e., racks, logs, dry, ice, shipping supplies).
� QAs tube/container labels before and after specimen collection.
� Schedules lab specimen pickup or transport of safety labs to hospital laboratory.
� Supports the Laboratory Coordinator and Supervisor with day to day protocol processing requirements as assigned.
� Assumes responsibility for accurate documentation (PK Logs, Flowsheets, lab requisitions, labels, etc.).
� Maintains daily upkeep of all lab areas (equipment is stored away, source documents are organized and filed, decontamination of lab work benches, etc.)
� Ensures all medical equipment (i.e., freezers, mechanical pipettes, centrifuges, refrigerators etc.) are functioning properly and have updated maintenance records.
� Maintains organization of contents of freezers/refrigerators at all times.
� Attends protocol specific training as assigned (including any specialized procedures, equipment, or processing).
� Attends regular laboratory staff meetings.
� Performs all other duties as assigned.

Skills:
� Must have strong interpersonal, written/verbal communication and organizational skills.
� Must have knowledge and skill in techniques of good clinical judgment.
� Must have the ability to effectively manage time and the ability to multi-task.
� Must demonstrate the knowledge and skills necessary to provide care appropriate to the age and/or indication of the study participants.

Education:
� BA/BS in Science-related field or equivalent lab experience preferred
� Valid Phlebotomy Certification or a California State License preferred

.
Language Skills:
� English

Minimum Work Experience:
� 1-2 years of clinical lab bench experience from a clinical or research lab setting
� Valid CPR certification
� Flexible schedule
� Local travel: Valid California Driver�s License and/or reliable transportation
� Ability to lift up to thirty (30) pounds

HOW TO APPLY:

Go to www.parexelcareers.com
Click on �Opportunities� (accept terms of usage to continue)
Search for the job by Location only (ex: USA-California-Glendale) then click �Submit�
Choose desired job
Click on �Add to Job Cart�
Click �Respond to all Jobs in Cart�
Click on �Respond to All Jobs in Cart�
Complete all required fields with the appropriate information about yourself

Scientific/Research & Development (Los Angeles)

2009-11-06T12:09:55-08:00

Clinical Research Nurse III (Los Angeles, CA)

2009-11-05T18:26:37-08:00

Join an International Leader in Pediatrics.
Childrens Hospital Los Angeles is a special place where children have been cared for and cured for more than 100 years. Our hospital has become one of the world�s top pediatric facilities, acknowledged throughout the United States and around the world for our leadership in pediatric and adolescent health.

With its �Magnet Recognition� for Nursing Excellence, the American Nursing Credentialing Center has made �official" what so many of our patient families, and those within the profession, have come to know - that this hospital is very, very special place, and its nurses are, too.

B.S.N.
Job Purpose and Summary: The Clinical Research Nurse III (CRN III) is a registered nurse who shares responsibility with the principal investigators to ensure that clinical investigations are conducted in accordance with the requirements of all regulatory agencies. The CRN III ensures that activities and approvals required for the protection of human subjects by the IRB (entitled "Committee on Clinical Investigations" at CHLA) are completed, that required data and documents are completed, that patients and families are prepared for participation in clinical protocols, and that effective methods for protocol management are used in collaboration with the attending MDs and other members of the research team. The CRN III oversees the direct nursing care provided by other licensed/non-licensed personnel in the research area, and supervises all aspects of clinical trials. Monitors study patients, provides nursing services, and maintains and oversees accurate records. Employee will follow applicable policies and procedures in handling supplies, pharmaceuticals, and equipment.

If you are interested in working with the very best physicians, surgeons and nurses, in a place where kids come first please visit our website www.childrenshospitalla.org

To Apply for this position, please CLICK HERE

Field Service Engineer - Medical Device (Any CA location)

2009-11-05T06:36:49-08:00

ANY WEST COAST LOCATION WILL BE CONSIDERED

Company Description:
InfraReDx, Inc. is a science-based medical device company with expertise in technologies useful for characterization of coronary plaques. The company first developed a system utilizing near-infrared spectroscopic (NIRS) technology to identify plaque composition. It has now developed IVUS technology to provide complementary information about the structure of plaques. The company, located in Burlington, Mass., was founded in 1998 to meet the unmet medical need for detection and identification of lipid core containing plaques of interest in the coronary arteries.

Responsibilities include:
� Completing regularly scheduled Preventive Maintenance calls, new product installations and customer service requests on medical imaging equipment
� Managing repair parts inventory while maintaining proper cycle counts
� Completing Functional Inspections on designated equipment
� Maintaining customer service logs and information and internal service records
� Training Cath Lab staff (physicians, nurses and technicians) on the proper use of the product; highlighting any changes on product upgrades
� Managing tools and test equipment inventory ensuring diagnostic tools are properly calibrated as required
� Utilizing Infraredx CAPA process to resolve customer service delivery issues and conducting root cause analysis that will lead to effective problem solving

Desired:
� Past experience in Field Service troubleshooting electro-mechanical devices and responding to customer service needs
� Excellent computer skills, including the diagnosis and repair of problems
� Excellent analytical and communication skills with the ability to communicate complex technical issues in an easy to understand manner
� Experience interfacing with both internal team members and external customers as part of a solution based service process
� Experience diagnosing and repairing medical imaging equipment in the Healthcare Industry
� Exceptional skills as a change agent and process oriented individual
� Dependable: Being reliable, responsible, dedicated, committed, and fulfilling obligations

Qualifications/Requirements:
� Bachelors degree, Electrical Engineering, Electrical Engineering Technology, equivalent military education or Associates degree with a minimum of 3 years experience servicing medical imaging equipment, or a High School Diploma/GED and a minimum of 10 years experience servicing electronic equipment
� Willingness to travel 75% within specified geographic regions
� Must have a valid driver's license

Skills Desired:
� Past experience in Field Service troubleshooting electro-mechanical devices and responding to customer service needs
� Excellent computer skills, including the diagnosis and repair of problems
� Excellent analytical and communication skills with the ability to communicate complex technical issues in an easy to understand manner
� Experience interfacing with both internal team members and external customers as part of a solution based service process
� Experience diagnosing and repairing medical imaging equipment in the Healthcare Industry
� Exceptional skills as a change agent and process oriented individual
� Dependable: Being reliable, responsible, dedicated, committed, and fulfilling obligations

Qualifications/Requirements:
� Bachelors degree, Electrical Engineering, Electrical Engineering Technology, equivalent military education or Associates degree with a minimum of 3 years experience servicing medical imaging equipment, or a High School Diploma/GED and a minimum of 10 years experience servicing electronic equipment
� Willingness to travel 75% within specified geographic regions
� Must have a valid driver's license

PLEASE COMPLETE ONLINE APPLICATION AND SUBMIT RESUME AT: https://home.eease.com/recruit/?id=38085

Growing Medical Marketing Firm Seeks New Service and Support Tech (East San Gabriel Valley)

2009-11-04T15:57:34-08:00

SYNOPSIS:

An Established medical marketing firm is growing and looking for experienced repair technicians who are self-motivated and hard working individuals. This job will begin as a part time position and grow into a full time position with the right skill sets and experience.

QUALIFICATIONS:

- Good customer service skills are a must!!!

- You will be required to listen to, learn and follow detailed instructions

- A good candidate must be self-motivated and have the ability to work with little or no supervision while still being a team player

- Basic computer knowledge is a must

- Requires a reliable car with insurance and a clean driving record

- Posseses the ability to troubleshoot, identify, and resolve a mechanical problem

- A mechanical background is desired, but will train the ideal candidate

Seasonal Naturalist (Calabasas, CA)

2009-11-04T15:39:29-08:00

Mountains Recreation and Conservation Authority

Seasonal Naturalist Position Spring 2010
Contract Duration: February 1st � June 11th, 2010

The Mountains Recreation and Conservation Authority is a local government agency founded in 1985. Our mission is to complement the work of other agencies protecting land in the Southern California Mountains by using our unique ability to acquire and improve parkland, afford educational opportunities, and provide stewardship for a wide variety of public park and open space amenities. The Outdoor Education School at King Gillette Ranch is a residential outdoor education program that provides a safe, challenging, fun, and dynamic program for 5th and 6th graders from throughout Southern California.

The seasonal naturalists with the MRCA will use the California State Curriculum Standards and established curriculum as guides in personalizing their classes. Seasonal naturalists will typically teach two 3-hour lessons during the day (one during the morning and one in the afternoon). Naturalists will also be responsible for:
� Teaching 2-3 evening programs per week
� Assisting with meals throughout the week
� Maintaining accurate records of incidents, injuries, and group behavior
� Actively participating in the overall program, including operations and staff meetings
� Assisting with student orientation, arrival, and departure
� Other duties as assigned

Qualifications
� BA or BS in related field
� A minimum of 1 year teaching in a residential environmental education setting
� Understanding of, and ability to communicate, ecological, recreational, and conservation concepts
� Passion for teaching and developing positive relationships with students
� Current First Aid and CPR certification
� Knowledge of the local flora and fauna of the Santa Monica Mountains
� Flexibility, high energy, self-motivation, and a huge commitment to teamwork
� Ability to be a positive member of a community that will live and work together

Compensation and Benefits
� Starting salary between $325-$375/week, depending upon experience
� Community living (a shared room/bath, common living room, kitchen, and free on-site laundry facilities) in a beautiful park setting in the Santa Monica Mountains
� Access to extensive trails, camping, beaches, and all the wonders that Southern California has to offer
� Extensive training and professional development
� Full-time, year-round naturalist positions may be available to exceptional staff upon completion of seasonal contract
� Caring, fun and experienced co-workers!

How to Apply

Please email the following to the Director of Camp Programs at jess.kohring@mrca.ca.gov or mail to Attn: Jess Kohring, King Gillette Ranch, 26800 Mulholland Highway, Calabasas, CA 91302. Application deadline: December 15th, 2009

� Cover letter
� Resume
� Three professional references

Catheter Engineer (Long Beach)

2009-11-03T15:12:23-08:00

Medical device startup is looking for an experienced catheter engineer. Candidate should be able to handle all aspects of device design including component design, packaging, project management, and preclinical protocol design. Experience with cardiology, electromechanical devices, design controls, and drug delivery is a plus. Company is located in Long Beach. Position can be contract or full time based. Minimum qualification includes a bachelor's degree in engineering and previous experience with medical device products/ technology.

Please email resume for consideration.

Environmental Technician (Los Angeles )

2009-11-03T11:25:50-08:00

Environmental Technician

We are seeking an Environmental Technician to perform groundwater monitoring as well as operation and maintenance of remediation systems. Must be able to work independently. Minimum of 3 - 5 years of experience only.

� Operate and maintain soil and groundwater remediation systems

� Troubleshoot electrical and mechanical problems

� Collect vapor and water samples

OSHSA 40 hour HAZWOPER training preferred.

ICP Process Development Chemist (Whittier, CA)

2009-11-03T10:52:29-08:00

BioPhase Solutions specializes in recruiting top talented professionals for Los Angeles and Orange County's scientific community. We are currently looking for a R&D Chemist to work for an Los Angeles area biotechnology company.

R&D Chemist

ESSENTIAL DUTIES:

� Designs and develops new products, applications or new processes for the Recycling Department.
� Is responsible for the reduction of accidents (occupational, reportable, recordable and minor) in the department to zero.
� Supports the introduction of the QM 9001 2000 and DIN EN ISO 14001 system in the Recycling Production and R&D department.
� Assures Quality and documentation according to the QM 9001 2000 and DIN EN ISO 14001 standard in the department.
� Works with support staff to assure departments� adherence to quality, safety and environmental standards that exceed the industry minimum.
� Supports the production in the case of acute problems.
� Calculates the production costs of new and improved products.
� Assures the systematic information exchange between other RC R&D departments in order to avoid double R&D work and decrease R&D costs.
� Supports maintenance group in the case of acute problems and questions concerning material selection and corrosion resistance.
� Plans and coordinates projects for the development of new processes and products under special consideration of costs and time schedule.

RESPONSIBILITIES

� Responsible for the planning, installation, maintenance and servicing of the devices, machinery and equipment in the department pursuant to the legal regulations in force.
� Responsible for timely communication of information to the VP Quality and Regulatory Compliance or his designee regarding any planned changes and new investments (as relevant under environmental or occupational protection aspects
� Responsible for orderly recruitment, control and training of subordinates.
� Responsible for coordinating all activity related to fire protection.
� Responsible for coordinating with Safety for all employee medical concerns.
� Responsible for developing, communicating, and training of operational and working instructions.
� Responsible for immediate notification of any deviations from the operation in accordance with the regulations and of any industrial accidents to the Vice President of Regulatory Compliance or his designee.

EDUCATION and/or EXPERIENCE:

� An experienced R&D Chemist with appropriate industry experience, preferably in the precious metals industry.
� An energetic, forward-thinking and creative individual with high ethical standards and an appropriate professional image.
� A well-organized and self-directed individual who is "politically savvy" and a team player.
� An intelligent and articulate individual who can relate to people at all levels of an organization and possesses excellent communication skills.
� Master Degree in Chemistry, PhD or with a minimum of 5 years working experience in the field of PM compounds production and research and development.

Email your MS Word resume to Chris@biophaseinc.com

Please also visit www.biophaseinc.com to view additional opportunities in Southern California!

Industrial Production Manager (Thousand Oaks, CA)

2009-11-03T10:11:14-08:00

Amgen Inc. has an opportunity for a Senior Manager. Reqs. Bachelor�s deg. & 5 yrs. exp.; & recent exp. in dev. manufacturing strategies, technology, & innovation lifecycle mgmt. Job Location: Thousand Oaks, CA. Send resume referencing #73QNW6 to: Global Mobility, Amgen, Inc., One Amgen Center Drive, Mailstop 19-1-A Thousand Oaks, CA 91320. No phone calls or e-mails please. Must be legally authorized to work in the U.S. without sponsorship. EOE.

Asbestos Analyst (San Gabriel Valley)

2009-11-02T16:21:23-08:00

Asbestos Analyst-Optical

Need analyst with experience in the optical identification of asbestos in construction materials and soil. Applicants with university level coursework in geology preferred but experienced applicants with appropriate training courses are acceptable.

This is a full time position but part time availability will be given consideration if the hours of availability are sufficiently flexible.

Benefits include paid vacation and holidays and health insurance.

Chemist 17 [2009-1571] (Cypress, CA)

2009-11-02T14:23:19-08:00

Chemist 17 [2009-1571]

The incumbent analyzes the concentration of certain components in food sample. The incumbent must accurately prepare and process the sample to obtain the needed results. Utilize various instruments such as HPLC, GC, and AA to determine concentration of desired balances in the food sample.

Ideal candidate will possess a BS degree in Chemistry, Food Science, or related field and up to two years relevant work experience. This person will be responsible for the analysis of food products in a chemistry laboratory. Individual must be highly organized, flexible, and work well in a team environment.

For further information and to apply to the position, follow the link below.

Please have a current resume to submit when you click here to Apply Online.

Thank You

Technology and Patent Literature Research

2009-11-01T16:46:41-08:00

Immediate, Part-time, full-time, virtual: Earn potential rewards for scientific technical documents and develop valuable experience in the exciting field of patent literature research.

Article One Partners (www.articleonepartners.com) lists requests for articles, patents, research papers, product literature or any written information from anywhere in the world that describes particular technologies as of a historic date. Article One�s research projects are called Patent Studies.

There are over 20 studies listed for some of the most important technologies worldwide, such as pharmaceuticals (Lunesta, Levitra, Geodon etc.), telephone apparati (Speech Processing by RIMM), software (Twitter.com), wireless technology, and Blu-ray disc drives on the Playstation 3.

Article One Partners needs you to find documented information-- prior art. By searching for prior art, you gain the invaluable experience of researching scientific documents, earn profit-sharing points, and may earn up to $50,000 per study. More than twenty studies are currently offered for over $1,000,000 in compensation rewards. Rewards are distributed when Article One determines that the public written information you submit can show a patent to be invalid.

Begin work immediately, register at www.articleonepartners.com, browse the Studies (check your eligibility), and apply your knowledge, research and network to find Prior Art. Article One will review your submissions and tell you if you have earned the cash rewards. Your active participation in Article One will earn profit sharing points. (The profit-sharing plan is described in detail on our website.)

By joining and participating in the community, you earn profit-sharing points. To learn more, come visit us at articleonepartners.com and register for free as an advisor. Also, Article One Partners will soon be adding new studies soon, so by registering now, advisors can get a head start on submitting new prior art.

Article One Partners is a web-based patent research company that searches for prior art. Prior art refers to the entire body of publicly available information that can potentially invalidate a patent by showing that its ideas were known by the date of invention of the patent. Invalidating prior art shows that an invention described in the claims of a patent existed before a date of invention. Prior art can also be used to establish the strength of a patent.

The Studies list patents with a description of the technology and the historic date. Patents are granted because the U.S. Patent Office concludes that the description of the technology in the patent is the first in the world. But the Patent Office is limited in being able to research worldwide public information. Article One offers a citizen�s review to check whether the patent description is the first. If you show an earlier description, you can earn $50k and high profile press as a state of the art researcher for recognition in industry and career building.

The public written information is called Prior Art. The historic date by which the Prior Art must be dated is called �Latest Date for Prior Art.� Each Study links to a patent or patents, and provides a written description of the technology and the latest date for Prior Art.

- Reduce the monopoly pricing you pay for products covered by patents which should not have been granted, help to reform U.S. patent law � and get compensated for your efforts and the value of your knowledge!

****When you register at AOP, please use the registration code Craig.****

Do you have hands-on lab or sales experience in biology or microscopy? (LA area - your location)

2009-10-31T07:39:12-07:00

Our client, a life sciences company , has an immediate need as it seeks to grow in the cellular imaging/microscopy market. Currently, we seek individuals experienced in the laboratory with cellular imaging/microscopy applications, systems and/or software to conduct outbound calls to researchers as a follow-up to ongoing purchase needs.

The Cellular Science/Imaging consultant will ...
- Work from home as an independent contractor with flexible hours
- make successive outbound calls to researchers from a list of warm leads and previous customers provided by the client
- utilize the client�s preferred pitch in the approach to these leads
- update customer records and confirm interest on behalf of client
- Cellular Imaging Consultant does not need to complete the sales process - only confirm interest and collect related information.

Excellent Cellular Science/Imaging Consultant candidate will meet the following criteria:
- have education, laboratory or sales experience in the field of biology, microbiology, microscopy or cellular sciences
- direct experience in cellular imaging/microscopy hardware, software and/or applications a plus
- MS/PhD not required - but a plus
- Inside sales and/or sales experience a plus
- have a computer with broadband internet access (not provided by, or reimbursed by the company)
- Have availability of 10 to 40 hours per week between the hours of 8am and 6pm eastern time
- have basic computer skills
- have a reasonably quiet setting in which to work
- have excellent phone skills
- be exceptionally diligent and reliable
- be able to work independently

The Cellular Science Consultant will be provided...
- required software and software orientation
- Product/technology orientation
- Lead follow-up techniques orientation

This is an outstanding opportunity for someone that would like to work from home, needs schedule flexibility and who would like to grow with this new business. Please send a resume with a thoughtful description of why you are interested in this opportunity in the body of the email, including your specific experience in cellular sciences.

Medical device packaging expert

2009-10-29T17:48:03-07:00

Medical device startup seeks medical device packaging expert with at least ten years of experience with epoxy and integration of medical devices for part-time work.

We pay competitive rates. Immediate work is available.

Please send your resume, rates and a description of your work and experience in assembling very small ophthalmic devices.

Program Manager (CLS, MLT) (Van Nuys)

2009-10-29T17:25:19-07:00

Cangene Corporation, a Canadian biopharmaceutical company, is headquartered in Winnipeg, Manitoba and has approximately 800 employees in eight locations across North America. This includes the operation of four specialty plasma collection facilities located in Florida, Maryland, California and Manitoba. Plasma collected from these facilities is used to create life saving medications which are sold worldwide. Visit www.Cangene.com for more information.
Cangene Plasma Resources, is a specialty plasma donation facility that collects human blood plasma which is used to create life saving medications.

We have an exciting opportunity in our Van Nuys Plasma Center for a Program Manager.

POSITION SUMMARY:

The program manager is responsible to manage specialty plasma programs and is responsible to assist the center manager in the overall activities, as designated by the center manager, required to meet corporate short and long term operational objectives. Compliance with Regulatory and Corporate policies and procedures is essential to ensure and maintain donor, employee and product safety.

1) Manage Specialty plasma programs

2) Ensure and maintain Regulatory and Corporate compliance

3) Possess working knowledge of all functions and operations of the plasmapheresis center

4) Maintain a high quality medical facility

QUALIFICATIONS:

The candidate should have lab experience and some blood bank experience is preferred.

Current California license as a Clinical Laboratory Scientist, or Medical Lab Technician is preferred but not required.

Researchers (Las Vegas)

2009-10-29T09:48:44-07:00

Bigelow Aerospace Advanced Space Studies (BAASS), a sister company to Bigelow Aerospace, is a newly formed research organization that focuses on the identification, evaluation, and acquisition of novel and emerging future technologies worldwide as they specifically relate to spacecraft. BAASS is headquartered in Las Vegas, Nevada. We are seeking experienced scientists to join our research teams. If you are an inquisitive outside of the circle thinker, who is detail oriented and who is looking for a challenge, this is a unique and exciting opportunity to advance your career and to be a part of cutting edge research.

Numerous positions are available in various fields

Impressive candidates will need to have 10 or more years of research and hands on experience in the disciplines related to aerospace sciences, specifically including:

� propulsion

� astrophysics

� physics

� biochemistry

� nanotechnologies

� microbiology

� stealth technologies

� and the engineering disciplines

Several positions are also available for research scientists in the disciplines of:

� forensic pathology

� electromagnetic fields

� biological cognitive interaction

A Masters or PhD in a relevant field is a must. Candidates must qualify for secret and top secret clearances and must be willing to submit to a thorough background check.

For all positions, some travel � both nationally and internationally -- may be required.

BAASS offers excellent pay and a benefit package that includes: medical, dental, vision, PTO, and a 401k.

For more information or to submit an application, go to http://www.bigelowaerospace.com/ or Mail your CV/Resum� to Attn. Donna @ 4640 S. Eastern Ave. Las Vegas, NV 89119 or fax to 702-456-9404.

Microbiology Environmental Monitoring (Los Angeles, CA)

2009-10-28T21:24:44-07:00

Microbiology Quality Lab Associate I - Los Angeles, CA 90039

Requirements:
-Must have Bachelor's Degree in the Biological Sciences with Microbiology emphasis
-Must have 2-3 years of industry experience
-Must have previous industry experience with environmental monitoring and aseptic techniques
-Must have good written and verbal communication skills
-Must be able to read and follow detailed written instructions
-Must have good interpersonal skills and be able to work effectively and efficiently in a team environment.

Responsibilities include:
-Perform microbiological testing (in-process/water testing, environmental monitoring and plate reading).
-Perform non-viable air, viable air, surface in aseptic filling in ISO 5 and 7, manufacturing bulk areas in ISO 8 and 9.
-Collect water in bulk manufacturing and test water via membrane filtration.
-Perform ECRs testing, plate reading, BI testing.
-Troubleshoot instruments and perform computer based analyses
-Perform review of test data, including overall documentation practices
-Perform release functions in LIMS or other computerized systems
-Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR, and cGMP regulations
-Investigate deviations and write exception documents
-Perform laboratory audits as required; audit and update SOPs as required and initiate document change requests

RESPOND HERE! To respond immediately, access the online response form at: http://sh.webhire.com/servlet/resp/rf?jobid=2372403&boardid=1904

Laboratory Assistant for Cryobank (Westwood, CA)

2009-10-28T16:43:10-07:00

Make a difference as a Laboratory Assistant by helping others to fulfill their dreams!

Building Families of Choice Since 1996

We are looking for someone with energy, inspiration, and a commitment to making a difference, who wants to work in an exciting, fast-paced and expanding organization.

Job Requirements

� Medical Assistant diploma
� Phlebotomy California license
� Good English oral and written communication skills
� Calm demeanor
� Ability to follow through on various tasks
� Ability to lift 40 pounds
� Ability to work in a team environment
� Extensive use of computer and phone
� Able to problem solve, plan and organize
� Punctuality and dependability are a must

Benefits

� Compensation $12 to $15 hour BOE
� Health insurance
� Paid parking or commuting stipend
� Retirement plan
� Educational scholarships
� Generous paid time off plan

For more company information go to: www.growinggenerations.com, see Sperm Donor Program section.

Please submit cover letter and resume to Teo Martinez, COO, through Human Resources at byron@growinggenerations.com. Attachments must either be in Microsoft Office Word or as a PDF
Please no phone calls or drop ins.

Be part of the satisfaction of Lives Created * Worlds Changed

Fertility Cryobank and its affiliate company, Growing Generations, are organizations passionately dedicated to the vision of creating life and, in the process, changing the world. The companies' mission is simple - to build families of choice around the world through surrogacy, egg donation and sperm donation. The company is a recognized leader in providing services to a wide range of family types including gay and lesbian, heterosexual, single, and persons with HIV.

START-Environmental Professionals (Long Beach, CA)

2009-10-28T11:25:07-07:00
Environmental Professional

Job summary: Ecology and Environment, Inc., an international environmental consulting firm, is offering exciting opportunities for environmental professionals to join our team working exclusively to support the USEPA Superfund Technical Assessment and Response Team (START) contract and manage a broad range of time-critical, hazardous materials investigations and Homeland protection-oriented activities out of our Oakland or Long Beach, California offices.
Responsibilities:
� Operation of environmental sampling/monitoring equipment
� Travel, emergency on-call and outdoor field work
� Planning, conducting, managing, and reporting on field assessments for hazardous materials
Requirements:
� Minimum, BA/BS in biology, geology, environmental science, chemistry, environmental engineering, or related discipline
� Minimum, 3 years experience with an environmental consulting firm or government agency and significant experience leading field projects
� Experience writing sampling/work plans and analyzing and presenting data in formal reports
� OSHA 40-hr training
� Familiarity with EPA analytical methods and knowledge of federal environmental regulations
� Excellent written and oral communication skills
� Excellent computer skills

E & E offers opportunities for growth in a team-oriented environment, competitive benefits package; including medical, dental, 401k and retirement plan. Please view our website at www.ene.com to apply on-line. Join our team and make a difference!

Environmental Professional (subcontractor) (Los Angeles)

2009-10-28T06:08:08-07:00
Environmental Professional (subcontractor)

Position Description
EBI Consulting is seeking Environmental Professionals on a part-time/contactor basis to complete Phase I Environmental Site Assessment reports and/or wireless National Environmental Policy Act (NEPA) reports throughout the United States. The work will require completion of field inspections of various property types, primarily sites under consideration for telecommunications installation as well as completion of independent research of local, state, and federal resources in compiling the information required for Phase I ESAs and NEPA Related Reports. In addition, screening for Lead Containing Pain and Asbestos may be required.

Experience Required
Prior experience with Phase I Environmental Site Assessments and NEPA Reports conducted for wireless carriers, tower companies, acquisition firms, or lenders.

A professional science degree in environmental science, ecology, biology, geology, engineering, or related field, and over two years professional experience in NEPA consulting and/or due diligence.

An understanding of and experience with NEPA reviews for proposed construction projects, including evaluating impacts to floodplains, wetlands, endangered species habitats, and historic properties
LBP and ACBM Certifications a PLUS.

Submittal
Please submit a resume and cover letter in Word or PDF format via email to jobs@ebiconsulting.com. You must include the following information:

1. Reference job #, job title and resource
2. Brief summary of past related experience (highlight your experience as it relates to our need & industry);
3. List of your education credentials and professional registrations
4. Salary history

We look forward to hearing from you!

Dairy Technician (Commerce)

2009-10-27T10:44:53-07:00
Michelson Laboratories, Inc. is a food/environmental testing laboratory located in the City of Commerce.

We are looking for a qualified candidate to perform analyses on dairy and dairy-related samples. Applicants having completed some college level science (biology/chemistry) with a Bachelors Degree in the Sciences are preferred but not necessary. Experience in a food-science laboratory or related field a plus.

This is a full-time position.
Serious applicants only.

Oncology Immunoassay Research Associate (West LA)

2009-10-27T09:57:46-07:00
Oncology Immunoassay Research Associate - Los Angeles, CA

This is a great scientific R&D position responsible for contributing to the development of Oncology monoclonal antibody therapeutics. You will also be responsible for developing, validating, and characterizing immunoassays, and cell-based assays including FACS, immunofluorescence, and immunoprecipitation assays. You will also be responsible for target discovery, target validation, screening, and signal transduction activities.

Preferred Candidate Background and Expertise:

* BS or MS degree in Biology, Biochemistry, Molecular Biology, Protein Biochemistry, or related Life Science field.
* Hands on expertise working with immunoassays and assays including FACS, immunofluorescence, immunoprecipitation, and western blots.
* Expertise working with cell proliferation, migration, cell growth, motility, apoptosis, angiogenesys, morphogenesys, or adhesion assays a plus.
* Oncology pharmaceutical research experience a plus.
* Expertise working with monoclonal antibodies, mAbs and performing mammalian cell culture/tissue culture activities.
* Knowledge of RNAi, shRNA, or siRNA a plus.

PLEASE APPLY HERE - http://bit.ly/1vcWkg

Project Manager -Scientific Affairs (Los Angeles, CA)

2009-10-24T11:20:33-07:00
Seeking a Project Manager with knowledge of Intellectual Property, Clinical Trails and Scientific Affairs

Job Duties:
-Review scientific data and provides summaries for Intellectual Property (IP) projects and product development.
-Supervise, plan and manage scientific and clinical studies with local universities, institutes, and other research entities.
-Travels occasionally to conferences, manufacturing and clinical trial sites, trade shows, events, and conventions sponsored by our company.
-Additional responsibilities and projects may be assigned.
-Assists in writing books, product literature and other technical projects.

Requirements:

-Ph.D in Biochemistry, Biology, Nutrition, or other biological fields of study.
-Experience (during graduate program or post grad) in clinical trials.
-Must be able and willing to travel internationally.
-Proficient in Word, Excel, PowerPoint, and Outlook.

This is a full-time position. Please reply with a Word Doc Resume Attachment and your desired salary requirements for immediate consideration.

Nanofiltration Research Associate (Los Angeles, CA)

2009-10-24T00:16:44-07:00
Nanofiltration Research Associate - Los Angeles, CA 90039

Our client currently has a 3 month contract position available for a Nanofiltration Research Associate.

Responsibilities will include:
- Perform filter press filtration study in a pilot plant environment.
- Conduct and analyze experiments.
- Process and analyze results and data.
- Maintain laboratory documentation and records in a detailed and descriptive manner.
- Conduct regular communication and critical reviews of their data, methods, and protocols.

Qualifications:

- Ideal candidate will have a Masters Degree in Chemical Engineering
- Previous nanofiltration experience a must
- 4-5 years lab experience
- Process Development experience
- Preferred candidates will possess excellent problem solving and sound verbal and written communication skills.

This is a contract position. The work schedule is Monday through Friday, 8:00AM to 5:00PM, and the pay rate range is commensurate with experience.

RESPOND HERE! To respond immediately, access the online response form at: http://sh.webhire.com/servlet/resp/rf?jobid=2402611&boardid=1904

Instrument Validation Associate (Los Angeles, CA)

2009-10-24T00:06:08-07:00
Instrument Validation Associate - Contract through end of the year.
Los Angeles, CA 90039

Responsibilities
-Perform instrument validation on analytical equipment.
-Perform tests in the validation protocol.
-Analyze validation results and provide reccomendations on findings.
-Coordinate reporting of samples for all validation.

Qualifications
-Must have previous relevant instrument validation experience.
-Solid science background, understanding of analytical method principle and instrumentation.

Education:
-Bachelors of Science, or advanced degree (MS and PhD) is preferred

Physical Demands:
-Must be able to lift, push, pull and carry up to 50 lbs.
-In general, the position requires a combination of sedentary work and walking around observing conditions in the facility.

Working Environment:
-Must be able to work in controlled environments requiring special gowning. Will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet and body.
-Will work in a cold or wet environment -Will be working in a loud area that requires hearing protection and other protective equipment to be worn.
-Will work around chemicals such as alcohol, acids, buffers and celite that may require respiratory protection.

RESPOND HERE! To respond immediately, access the online response form at: http://sh.webhire.com/servlet/resp/rf?jobid=2404262&boardid=1904

Staff Research Associate - UCLA Family Medicine (910 North Vine Street, Los Angeles, CA 9)

2009-10-23T16:14:22-07:00
This job is being posted by the UCLA Department of Family Medicine. To apply for this job, search for job H50974 at https://jobs2.mednet.ucla.edu/css_external/CSSPage_Welcome.ASP.

Under the supervision of the Principal Investigator and Manager, this position will provide study coordination, recruitment, intervention delivery, qualitative data collection and coding, and general research support to all funded research projects. This person will also provide database assistance, study coordination, and general research support to the substance abuse and HIV-related research studies.
The ideal candidate will have a Bachelor's degree in a health-related field; be willing to work evenings and weekends as part of regular schedule. Have experience working in a community-based organization or with African American focused programs to address health disparities. Demonstrated sensitivity and familiarity with African American communities and culture. Be willing to be certified in HIV counseling and testing. Have experience working on HIV prevention in a health services or research setting and have experience with recruiting, enrolling, and delivering services or interventions to African American men who have sex with men. The candidate must have a valid California driver's license, access to a vehicle, and appropriate level of auto insurance.

Q.A. Technician (Santa Fe Springs)

2009-10-23T09:15:08-07:00
Job Description:
Review and approve Production Batch Record documents for ensuring dietary supplements meet identity, strength, purity and composition specification before commencement of production
Continuously monitor processes and review and approve test results of in-process and finished product at each critical control step
Monitor personnel hygiene and cleanliness, cleaning and sanitization of premises, facilities, equipments and utensils and ensure compliance.
Support QA Supervisor in auditing the manufacturing processes to ensure adherence to cGMPs and of sampling plans and measurements of samples and products
Determine and assure the specifications are met for any product and process
Preparation and review from regulatory perspective of label copy for dietary supplements
Analyze and apply FDA regulations for dietary supplements to the QA function.
Review formulas for accuracy against label claims.
Preparation, Reconciliation and Control of Production Documentation
Release of finished product
Conduct facilities inspections and internal audits to assure compliance with SOP�s
Participate in Company�s Continual Training Program
Keen attention to details of current procedures and adhere to established procedures
The employee will be assigned additional duties time to time as required by the Company

Knowledge:
Production and Processing: Knowledge of raw materials, production processes, quality control, regulatory affairs, costs, and other techniques for maximizing the effective manufacture and distribution of goods.
Mathematics: Knowledge of arithmetic, algebra, calculus, statistics, and their applications.
Customer and Personal Service: Knowledge of principles and processes for providing customer and personal services. This includes customer needs assessment, meeting quality standards for services, and evaluation of customer satisfaction.
Quality systems Implementation & Compliance: Specifically knowledge in ISO 9001-2000
Regulations: Some knowledge of regulations specific to our industry as FDA, GMP

Chemist for Project or Sales (updated) (San Gabriel Valley)

2009-10-23T03:15:08-07:00
Do you need a second job? We are looking for an entry-level or experienced chemist to help with a small project related to flavorings (research, creation, application, evaluation), liquid nutraceutical supplements, and energy drinks. Your expertise in any or all of these areas is required. If you like, you can also participate in our freelance sales program and earn industry-leading commissions.

Bachelor of Science in Chemistry is required. We have a new lab at a manufacturing/processing facility. Please email your cover letter and resume.

Staff Geologist (CA, Fullerton)

2009-10-22T21:36:32-07:00
When you work for ARCADIS, you are part of a bigger picture. You're a member of an international team of leading professionals. You work in a setting that allows you room to grow. ARCADIS offers everyone the possibility to develop and improve their own bigger picture.

ARCADIS is seeking a motivated Geologist to support a growing base of projects in our Orange Country Area office located in Fullerton, CA. This is an entry to junior level opportunity for a dynamic individual looking for career growth in environmental consulting. Fieldwork may include soil and groundwater collection, operation and maintenance activities for remediation systems, soil gas surveys, groundwater well installation, and Phase I and Phase II Environmental Site Assessments. Office work may include data compilation, report writing, and regulatory file review.

This position offers an opportunity to learn about a wide variety of environmental projects, work with a great team, and join a successful growing organization with a reputation for high quality work and top notch employees.

There are two positions open.

Position requirements include, but are not limited to:

* Minimum years of experience: 0-1

* Education required: BS in Geology, Hydrogeology, or another Geoscience

* Education preferred: MS in Geology, Hydrogeology, or another Geoscience

* This position does require travel. Travel amount is negligible and within S. California.

* A valid driver's license and clean driving record is required for this position.

* This position does not manage others

ARCADIS is an Equal Opportunity Employer M/F/D/V

RESPOND HERE! To respond immediately, access the online response form at: http://sh.webhire.com/servlet/resp/rf?jobid=2402585&boardid=1904

Plasma Technician (Van Nuys, CA)

2009-10-22T12:21:02-07:00
Cangene Corporation, a Canadian biopharmaceutical company, is headquartered in Winnipeg, Manitoba and has approximately 700 employees in eight locations across North America. This includes the operation of four specialty plasma collection facilities located in Florida, Maryland, California and Manitoba. Plasma collected from these facilities is used to create life saving medications which are sold worldwide. Visit www.Cangene.com for more information.
Bio Therapeutic Laboratories is a specialty plasma donation facility that collects human blood plasma which is used to create life saving medications. We
have an exciting opportunity for the right candidate to join our team in a rapidly growing environment as a Plasma/Donor Technician.

Essential Duties and Responsibilities:

• Donor Screening-Determine donor suitability in accordance with regulations, corporate policies.
• Product Collection-Perform the collection of Source Plasma and Whole Blood in accordance with applicable Regulations.
• Efficiently monitor donors through the donation process to avoid trauma.
• Product Processing-Perform proper receipt and processing of collection products. Complete accurate documentation for all products collected. Perform sample processing and pooling procedures. Prepare products for shipping in accordance with Regulations and SOP's.

Desired Minimum Qualifications
Education and Experience:
• Minimum High School Graduate or equivalent.
• Current CPR card.
• Phlebotomist certificate or equivalent experience (1 year)
• Knowledge of FDA, CLIA, OSHA and QPP regulations applicable to the qualification and donation process of donors as well as the processing and storage area.

***Plasmaphersis experience is preferred.

Program Manager (Van Nuys)

2009-10-22T12:17:50-07:00
Cangene Corporation, a Canadian biopharmaceutical company, is headquartered in Winnipeg, Manitoba and has approximately 700 employees in eight locations across North America. This includes the operation of four specialty plasma collection facilities located in Florida, Maryland, California and Manitoba. Plasma collected from these facilities is used to create life saving medications which are sold worldwide. Visit www.Cangene.com for more information.

Cangene Plasma Resources, is a specialty plasma donation facility that collects human blood plasma which is used to create life saving medications.
We have an exciting opportunity in our Van Nuys Plasma Center for a Program Manager. PLASMA OR BLOOD BANK EXPERIENCE A MUST!

POSITION SUMMARY:
The program manager is responsible to manage specialty plasma programs and is responsible to assist the center manager in the overall activities, as designated by the center manager, required to meet corporate short and long term operational objectives. Compliance with Regulatory and Corporate policies and procedures is essential to ensure and maintain donor, employee and product safety.

1) Manage Specialty plasma programs
2) Ensure and maintain Regulatory and Corporate compliance
3) Possess working knowledge of all functions and operations of the plasmapheresis center
4) Maintain a high quality medical facility

QUALIFICATIONS:

1. Must hold a current California license as a Registered Nurse, Family Nurse Practitioner, or Physician Assistant. Current certification in Cardiopulmonary Resuscitation (CPR) is required.
2. Must be able to read, write and follow oral or written instructions (English).
3. Knowledge of FDA, CLIA, OSHA, and QPP regulations applicable to the qualification and donation process of donors as well as the processing and storage area. Plasmapheresis experience is preferred.

Biopharmaceutical Investigator (Los Angeles, CA 90039)

2009-10-21T21:35:21-07:00
Biopharmaceutical Investigator - Los Angeles, CA 90039

Summary
-Support investigation of exceptions by determining root cause, performing data mining and providing recommendation of corrective actions. The investigator will learn all aspects related to manufacturing, Quality and release of products.

Responsibilities
-Learn to make Quality decision on the product and process -Investigate exceptions and deviations -Coordinate and lead personnel from manufacturing (from technicians to management), Quality, Technical Service, as well as Engineering, to ensure proper closure of exceptions that hold products and appropriate assignments of corrective actions, -Identify coding errors in PLC or Delta V that contribute to root cause of exceptions -Present the summary of exceptions - including root causes and corrective actions - to Quality, Manufacturing and/or Engineering -Understand the role of change control in pharmaceutical manufacturing -Understand the process and impacts of deviations and/or changes made to the process or equipment to downstream process, as well as final container products -Learn to analyze trends through statistical tools.

Requirements
-Bachelor's degree in Engineering or Chemical Engineering -Ability to communicate effectively to all levels of personnel - technicians, supervisors/managers, directors, engineers and scientists -Organization and multi-tasking skills - ability to lead, coordinate, manage and prioritize based on criticality of the situation/projects -Reliability - ability to perform the assigned tasks independently with minimal supervision -Basic knowledge of computer language and separation processes -Ability to troubleshoot equipment -Ability to work under pressure -Ability to work overtime as needed -Technical writing skills -Teamwork mentality, interpersonal skills

RESPOND HERE! To respond immediately, access the online response form at: http://sh.webhire.com/servlet/resp/rf?jobid=2388335&boardid=1904

Laboratory Office Assistant (Sylmar)

2009-10-21T18:30:11-07:00
Pacific Coast Analytical Services, a.k.a. PCAS , has an immediate opening for a part time office assistant at our office in Sylmar, CA. If you are looking to work with a dynamic group, grow to your fullest potential, and be part of an exceptional team PCAS is the place for you. PCAS is an independent testing laboratory founded in 1992. More info at: www.pacificcoastanalytical.com.

Job Description: Typing lab reports and maintaining regulatory records. Answering phones and interacting with customers and employees. Support basic accounting activities including invoicing and collections. Ordering chemicals and supplies. Preparing internal documents. Performing sales cold calls.

Qualifications:
► Detail oriented. Data entry experience REQUIRED.
► Microsoft Word and Excel REQUIRED. Quicken & Quickbooks is a plus.
► Accurate typing/data entry skills. Must type at least 40 to 45 WPM. REQUIRED.
► Must be SELF-MOTIVATED and RELIABLE
► High school REQUIRED. Science degree and fluency in Spanish is a plus.
► Phone sales experience is a plus.
► US citizen/resident or legal working visa REQUIRED.
► Lab tech experience is a plus.

Compensation: Minimum wage. Position is part-time with no benefits.

PCAS does not pay relocation expenses for this position. To apply please e-mail resume. DO NOT CALL.

QC R&D Chemist (Pomona, CA)

2009-10-21T16:07:00-07:00
Biophase Solutions specializes in placing the top talented professionals in the leading Biotechnology and Pharmaceutical Companies in Southern California. We are currently recruiting for a QC Chemist to work for a Pharmaceutical Company in Pomona, CA.

BS or MS in Chemistry

Must have 2+ years experience working in the Pharmaceutical industry and be familiar with FDA/ISO/GMP procedures.

Should be familiar with:
Gas/Liquid Chromatography
Mass Spectrometry
Ion Chromatography
Nuclear Magnetic Resonance
FT-IR Spectroscopy
UV-VIS Spectroscopy
Rheometry
Refractometry
Polarimetry
Thin Layer Chromatography
High Performance Liquid Chromatography
SDS-PAGE
Western Blot

Contract to Hire (3 months contract)
Salary up to 50K
Monday-Friday 8AM-4:30PM

Please send your resume to Chris@biophaseinc.com along with a brief cover letter explaining your qualifications

Medical Research (Marina Del Rey)

2009-10-21T15:05:05-07:00

Doctor Evidence, based in Los Angeles, builds databases of evidence for clients such as medical societies, medical manufacturers, journals, hospitals and other healthcare companies. We have a revolutionary technology that is positioned to transform the evidence-based medical space, and we are looking to hire people interested in translating and analyzing clinical studies.

The ideal candidate would be:

� A pre-medical student/recent college graduate with experience at analyzing clinical studies.

To be considered for this position a strong disposition to computer technology is a must! All prospective applicants must also reside in the Los Angeles area. This is a full-time position offered with competitive pay. If you are interested, please visit our website at www.doctorevidence.com to learn more about the company and our mission.

Address CVs/Resumes to Chris: cyu@doctorevidence.com.

Vet/ Kennel Assistant (hollywood/wilshire/hancock park)

2009-10-20T09:12:33-07:00
Busy 4 doctor small animal pratice located in Larchmont is looking for eager, friendly, ready to learn veterinary assistants for a part-time postion. Duties would include but not limited to helping doctors/techs, handling animals, cleaning up after animals, assist clients, and maintance of the clinic. Hours would be several days a week from 4:30pm til 6:30pm, Saturday's 9am til 4:30pm, and a one or two Sunday's per month. Perfect job for a student! Experince is not required but prefered, willing to train the right person. Please contact at larchmontac@sbcglobal.net

Per Diem Laboratory Technician (Glendale, CA)

2009-10-19T15:38:41-07:00
California Clinical Trials, subsidiary of PAREXEL International, is searching for a qualified and energetic Lab Technician to join a great team of researchers. The Lab Technician performs all duties related to serving as a lab technician for the Early Drug Development, Phase II-IV, and Sleep Departments. This position reports to the Laboratory Supervisor.

Major Responsibilities
Including but not limited to the following and other duties as may be assigned:

' Possesses detailed knowledge of study protocol lab procedures.

' Collects, processes and ships safety labs and pharmacokinetic (PK) samples according to clinical study protocol.

' Organizes hospital lab set-up and supplies (i.e., racks, logs, dry, ice, shipping supplies).

' Assists with daily lab supply list per protocol in conjunction with the Senior Lab Associate.

' QAs tube/container labels before and after specimen collection.

' Schedules lab specimen pickup.

' Contacts CRC/SCRC/Manager to confirm arrival of specimen shipments.

' Attends EDD/Phase II-IV/Sleep Dept. Meetings as appropriate.

' Acts as lab technician for EDD/Phase II-IV/Sleep Departments.

' Assists EDD Department with documentation (i.e., CRFs, lab requisitions, etc.).

' Performs routine upkeep of lab.

' Maintains and updates knowledge of Clinical Operating Guidelines and their proper application.

All other duties as assigned.

Qualifications:

Valid Phlebotomy Certification or a California State License.
Valid CPR Certification.
1-2 years hospital/lab phlebotomy experience.
Computer proficiency required.
Flexible schedule.
Local travel required: valid California Driver's License and/or reliable transportation.
Ability to lift up to thirty (30) lbs.

Competencies and Best Practice for High Performers:

Meticulous attention to detail.
Strong interpersonal, written/verbal communication and organizational skills.
Must have the ability to effectively manage time and the ability to multi-task.
Functions well in a Team environment.

HOW TO APPLY:

Go to www.parexelcareers.com
Click on �Opportunities� (accept terms of usage to continue)
Search for the job by Location only (ex: USA-California-Glendale) then click �Submit�
Choose desired job
Click on �Add to Job Cart�
Click �Respond to all Jobs in Cart�
Click on �Respond to All Jobs in Cart�
Complete all required fields with the appropriate information about yourself

Environmental Microbiologist-Mycologist-Aerobiologist (Los Angeles Area )

2009-10-19T13:51:25-07:00
Environmental Company is seeking full time Microbiologist/Mycologist/Aerobiologist for is busy growing laboratory located in the Los Angeles Area. This position is full time and offers a competitive salary for those with direct commercial environmental microbiology experience, especially those with experience working in an AIHA accredited laboratory.

This position involves microbial and bioaerosol analysis of samples for fungi and bacteria. The successful candidate must be familiar with all daily activities in the laboratory, including analyzing samples, maintaining the QA/QC Program and Standard Operating Procedures.

Requirements:
MS or B.Sc. in Mycology/Microbiology with strong background in Mycology.
Experience in Environmental testing of bioaerosols and microbial analysis.
Applicant must be able to enumerate, identify and confirm a wide variety of bacteria and fungi.
Minimum of 3 years experience in testing of bioaerosols and microbial analysis.
Must be able work work well with others in a team setting and also independently
Must have excellent communication skills will have contact daily on the phone with clients

Position offers benefits: medical/dental, 401(k), paid time off, holidays, voluntary benefits etc.

EOE

ICP Process Development Chemist (Whittier, CA)

2009-10-19T13:44:02-07:00
BioPhase Solutions specializes in recruiting top talented professionals for Los Angeles and Orange County's scientific community. We are currently looking for a R&D Chemist to work for an Los Angeles area biotechnology company.

R&D Chemist

ESSENTIAL DUTIES:

� Designs and develops new products, applications or new processes for the Recycling Department.
� Is responsible for the reduction of accidents (occupational, reportable, recordable and minor) in the department to zero.
� Supports the introduction of the QM 9001 2000 and DIN EN ISO 14001 system in the Recycling Production and R&D department.
� Assures Quality and documentation according to the QM 9001 2000 and DIN EN ISO 14001 standard in the department.
� Works with support staff to assure departments� adherence to quality, safety and environmental standards that exceed the industry minimum.
� Supports the production in the case of acute problems.
� Calculates the production costs of new and improved products.
� Assures the systematic information exchange between other RC R&D departments in order to avoid double R&D work and decrease R&D costs.
� Supports maintenance group in the case of acute problems and questions concerning material selection and corrosion resistance.
� Plans and coordinates projects for the development of new processes and products under special consideration of costs and time schedule.

RESPONSIBILITIES

� Responsible for the planning, installation, maintenance and servicing of the devices, machinery and equipment in the department pursuant to the legal regulations in force.
� Responsible for timely communication of information to the VP Quality and Regulatory Compliance or his designee regarding any planned changes and new investments (as relevant under environmental or occupational protection aspects
� Responsible for orderly recruitment, control and training of subordinates.
� Responsible for coordinating all activity related to fire protection.
� Responsible for coordinating with Safety for all employee medical concerns.
� Responsible for developing, communicating, and training of operational and working instructions.
� Responsible for immediate notification of any deviations from the operation in accordance with the regulations and of any industrial accidents to the Vice President of Regulatory Compliance or his designee.

EDUCATION and/or EXPERIENCE:

� An experienced R&D Chemist with appropriate industry experience, preferably in the precious metals industry.
� An energetic, forward-thinking and creative individual with high ethical standards and an appropriate professional image.
� A well-organized and self-directed individual who is "politically savvy" and a team player.
� An intelligent and articulate individual who can relate to people at all levels of an organization and possesses excellent communication skills.
� Master Degree in Chemistry, PhD or with a minimum of 5 years working experience in the field of PM compounds production and research and development.

Email your MS Word resume to Chris@biophaseinc.com

Please also visit www.biophaseinc.com to view additional opportunities in Southern California!

Laboratory Assistant at Cryobank (Westwood, CA)

2009-10-19T11:14:22-07:00
Make a difference as a Laboratory Assistant by helping others to fulfill their dreams.

Building Families of Choice Since 1996

We are looking for someone with energy, inspiration, and a commitment to making a difference, who wants to work in an exciting, fast-paced and expanding organization.

Job Requirements

� Medical Assistant diploma
� Phlebotomy license
� Good English oral and written communication skills
� Calm demeanor
� Ability to follow through
� Ability to lift 40 pounds
� Ability to work in a team environment.
� Extensive use of computer and phone
� Able to problem solve, plan and organize
� Punctuality and dependability are a must

Benefits

� Compensation $12 to $15 hour BOE
� Health insurance
� Paid parking or commuting stipend
� Retirement plan
� Educational scholarships
� Generous paid time off plan

For more company information go to: www.growinggenerations.com, Sperm Donor Program
Please submit cover letter and resume to Teo Martinez, COO through Human Resources byron@growinggenerations.com
Please no phone calls.

Be part of the satisfaction of Lives Created * Worlds Changed

Fertility Cryobank and its affiliate company, Growing Generations, are organizations passionately dedicated to the vision of creating life and, in the process, changing the world. The companies' mission is simple - to build families of choice around the world through surrogacy, egg donation and sperm donation. The company is a recognized leader in providing services to a wide range of family types including gay and lesbian, heterosexual, single, and persons with HIV.

CEO Assistant with Engineering or Bio Research Background. (Irvine)

2009-10-16T20:09:27-07:00

Innovative company seeks high-level EA for CEO. Applicant must have: BA or BS; engineering or medical/bio research experience; C-level assistant experience; ability to manage complex calendar, travel, meetings, and use MS Office (especially PowerPoint and Excel).

Cover, resume.
Photo requested by client for dossier presentation format, but not required.

Manager, Clinical Research Contracts (Los Angeles, CA)

2009-10-15T19:51:11-07:00

Join an International Leader in Pediatrics.
Childrens Hospital Los Angeles is a special place where children have been cared for and cured for more than 100 years. Our hospital has become one of the world�s top pediatric facilities, acknowledged throughout the United States and around the world for our leadership in pediatric and adolescent health.

With its �Magnet Recognition� for Nursing Excellence, the American Nursing Credentialing Center has made �official" what so many of our patient families, and those within the profession, have come to know - that this hospital is very, very special place, and its nurses are, too.

The Clinical Research Contracts Manager reports to the Administrator of Pre-Award Support Services in the Office of Research Advancement and Administration and has primary responsibility for the review, negotiation and execution of clinical research contracts. Ensures every contract provides the most favorable contractual and financial terms and conditions for the PI and CHLA. Collaborates with the Post-Award Financial Services for the fiscal oversight of clinical contracts, works closely with the Clinical Investigations Center (CLIC) to ensure all clinical research budgets are reviewed and accounted for in accordance with established (CLIC) policies and procedures. Acts as liaison representing the PI and division staff in negotiations and interactions with sponsors.

Qualifications:
Bachelor's degree required. Masters Degree or Jurist Doctorate preferred. Five years experience in clinical research contracts administration, including extensive experience in pre-award administration of clinical trial agreements with private and governmental entities. Two (2) years supervisory experience. (Preferred). Experience with the negotiation of large service contracts, and a minimum of five years experience in reviewing and negotiating Clinical Trial Agreements. (Required)

Knowledge, Skills and Abilities Required:
Excellent oral and written communication skills. Extensive knowledge and expertise related to all regulations regarding clinical research, including, federal, local and international, policies, procedures, circulars and laws applicable to clinical trial activity. In particular, FDA guidelines, GCP, OMB Circulars A 110, A 122, A 133, OASC 3, the PHS and NIH Grants Policy Statements. (Required) Extensive experience in pre and post award administration of biomedical grants & contracts, in particular with National Institutes of Health (NIH) grants and CDC. (Preferred) Familiarity with federal regulations, policies, procedures and circulars applicable to Research Institutional Committees. (Preferred) Experience in an academic research environment. (Preferred) Analytical skills to review, contracts and Clinical Trial Agreements against established criteria. Working knowledge of relational databases for management of grants & contract information. (Required) Experience in navigating and retrieving information from the Internet. (Required)

Childrens Hospital Los Angeles (CHLA) is a special place where children have been cared for and cured for more than 100 years. Our hospital has become one of the world's top pediatric facilities, acknowledged throughout the United States and around the world for our leadership in pediatric and adolescent health.
EOE/AA

If you are interested in working with the very best physicians, surgeons and nurses, in a place where kids come first please visit our website www.childrenshospitalla.org

To Apply for this position, please CLICK HERE

***Director of Pharmacy*** (Glendora)

2009-10-15T16:15:28-07:00
The Director of Pharmacy will oversee all pharmacy operations including planning, organizing, controlling and supervising activities in the hospital pharmacy according to hospital policies and standards of practice. The ideal candidate will have experience as Director or Manager of Pharmacy in a hospital. Ability to work independently, set priorities, make critical decisions and 2+ years of management experience a must.

Excellent Opportunity w/ competitive pay structure!

Please e-mail resumes to the above address,
or contact (626) 203-6861

R&D Chemist

2009-10-15T15:55:32-07:00
BioPhase Solutions specializes in recruiting top talented professionals for Los Angeles and Orange County's scientific community. We are currently looking for a Microbiologist to work for an Los Angeles area biotechnology company.

R&D Chemist

ESSENTIAL DUTIES:

� Designs and develops new products, applications or new processes for the Recycling Department.

� Is responsible for the reduction of accidents (occupational, reportable, recordable and minor) in the department to zero.

� Supports the introduction of the QM 9001 2000 and DIN EN ISO 14001 system in the Recycling Production and R&D department.

� Assures Quality and documentation according to the QM 9001 2000 and DIN EN ISO 14001 standard in the department.

� Works with support staff to assure departments� adherence to quality, safety and environmental standards that exceed the industry minimum.

� Supports the production in the case of acute problems.

� Calculates the production costs of new and improved products.

� Assures the systematic information exchange between other RC R&D departments in order to avoid double R&D work and decrease R&D costs.

� Supports maintenance group in the case of acute problems and questions concerning material selection and corrosion resistance.

� Plans and coordinates projects for the development of new processes and products under special consideration of costs and time schedule.

RESPONSIBILITIES

� Responsible for the planning, installation, maintenance and servicing of the devices, machinery and equipment in the department pursuant to the legal regulations in force.

� Responsible for timely communication of information to the VP Quality and Regulatory Compliance or his designee regarding any planned changes and new investments (as relevant under environmental or occupational protection aspects).

� Responsible for orderly recruitment, control and training of subordinates.

� Responsible for coordinating all activity related to fire protection.

� Responsible for coordinating with Safety for all employee medical concerns.

� Responsible for developing, communicating, and training of operational and working instructions.

� Responsible for immediate notification of any deviations from the operation in accordance with the regulations and of any industrial accidents to the Vice President of Regulatory Compliance or his designee.

EDUCATION and/or EXPERIENCE:

� An experienced R&D Chemist with appropriate industry experience, preferably in the precious metals industry.

� An energetic, forward-thinking and creative individual with high ethical standards and an appropriate professional image.

� A well-organized and self-directed individual who is "politically savvy" and a team player.

� An intelligent and articulate individual who can relate to people at all levels of an organization and possesses excellent communication skills.

� Master Degree in Chemistry, PhD or with a minimum of 5 years working experience in the field of PM compounds production and research and development.

Please also visit www.biophaseinc.com to view additional opportunities in Southern California!

Public Admin Analyst (Los Angeles)

2009-10-15T15:05:04-07:00
Under the supervision of the Principal Investigator of the AIDS Prevention and Treatment Clinical Trails Unit and the CARE Center Management Service Officer provide overall coordination and support of the multi-site, multi-network. Coordinate the clinical Research Site activities with various research protocols under different NIH funded Networks. Work to assure support from the central CTU while respecting the specific needs imposed by the Network/protocols that the CRS is working under. Assure coordination and accountability to primary funder as well as meeting the needs of UCLA and the ARRA act which funds this specific award. Write reports, grants, progress reports and correspondence realted to CTU and its Network CRSs. Oversee the CTU annual NIH format noncompetitive renewal. Prepare CTU related contract/grant proposals and continuation applications. Prepare Quarterly ARRA reports on the CRU per NIH and UCLA guidelines. Directly supervise the CTU Outreach Coordinator, work closely with the UCLA Operations Manager to develop standards and assure ongoing review of all UCLA and CTU employees.

QUALIFICATIONS: Knowledge of HIV disease. Working knowledge of regulatory systems relating to clinical trails. Experience with NIH grants, new and non-competing submissions, including budget development, coordination of documents, familiarity with paper 2590, 398 and electronic formats. Demonstrated ability to provide effective leadership and direction at all times. Ability to supervise. General knowledge of management principles, practices and their application in complex multi-institutional settings. Excellent communication skills. Ability to work some evenings and weekends in order to meet deadlines or attend meetings, events or conferences.

Postdoctoral Fellow (Duarte, California)

2009-10-15T07:12:53-07:00

Postdoctoral Fellow - Molecular Biology & Physiology

The collegial atmosphere at City of Hope provides unique opportunities for translational research, continuing education and professional achievement. We are a National Cancer Institute-designated Comprehensive Cancer Center and a leader in biomedicine. We invite you to collaborate with us.

We are seeking an experienced Research Fellow to join the laboratory within the Department of Gene Regulation and Drug led by Barry Marc Forman, M.D., Ph.D. The focus of the lab is to utilize orphan nuclear receptors to identify novel signaling pathways; to elucidate their molecular mechanism of action and to study their physiological effects.

Over the past few years, we have discovered several new signaling molecules that regulate critical molecular and cellular events including fat cell formation, glucose homeostasis and cholesterol metabolism and drug and sterol clearance. Among these recent discoveries was the identification of the first new steroid hormone to be discovered in 30 years. Thus, orphan receptors define exciting new areas of research, which have significant implications for both basic research, metabolic disease, diabetes, cancer and the design of new drug therapies.

Molecular biology, animal models and other techniques will be used including interactions with chemists and a variety of core facilities (high-throughput screening, mass-spec, etc.). Suitable candidates will have a Ph.D. with experience and potential in modern molecular biology and physiology.

To Apply: Please submit a statement of research interests and/or experience, a current curriculum vitae, and names and addresses of three references to Dr. Forman c/o Eileen Sepulveda: esepulveda@coh.org EOE/AA

For more information, visit our lab's web site at www.cityofhope.org/bforman/

At City of Hope, discovery and compassion work together - for life. To learn more about our organization and our opportunities, please visit www.cityofhope.org

KW: Los Angeles, California, LA, physiology, metabolism, molecular, signaling, nuclear receptors, receptors, cellular, cell, steroid, hormone, cholesterol

To qualify: The candidate must have a Ph.D.

Environmental Regulatory Specialist (Irvine, CA)

2009-10-15T02:12:03-07:00

ICF International (NASDAQ: ICFI) partners with government and commercial clients to deliver consulting services and technology solutions in the energy, climate change, environment, transportation, social programs, health, defense, and emergency management markets. The firm combines passion for its work with industry expertise and innovative analytics to produce compelling results throughout the entire program life cycle, from analysis and design through implementation and improvement. Since 1969, ICF has been serving government at all levels, major corporations, and multilateral institutions. More than 3,000 employees serve these clients worldwide. ICF's Web site is www.icfi.com

ICF International has joined forces with Jones & Stokes, one of the premier multidisciplinary environmental consulting firms in the western United States. For nearly 40 years, Jones & Stokes has supported a broad mix of federal, state, and local government and private-sector clients on infrastructure improvement projects, restoration and planning projects, and compliance with mandated government programs. ICF Jones & Stokes provides an array of integrated services in environmental planning and natural resource management, especially in the transportation, water, energy, and natural resources sectors. ICF Jones & Stokes� Web site is www.jonesandstokes.com

This full-time Environmental Regulatory Specialist position is located in our Irvine, CA office, and will work throughout the southern California region, with the potential for statewide involvement.

RESPONSIBILITIES:
In this role, you will be part of the Regulatory Compliance team and provide our clients with services that include all aspects of compliance with Sections 401 and 404 of the federal Clean Water Act, Section 10 of the Rivers and Harbors Act, Section 1600 of the California Fish and Game Code, and state and federal Endangered Species Acts. You will also provide jurisdictional delineations. Our current team members are highly skilled and motivated, and we are looking for additional support to serve our growing list of clients and projects.

BASIC QUALIFICATIONS:
� Bachelor�s degree in environment science
� 2+ years of regulatory compliance experience in the environmental or natural resources consulting industry required
� Jurisdictional delineation experience required

ICF offers an excellent benefits package, an award winning talent development program, and fosters a highly skilled, energized and empowered workforce.

ICF International is an Equal Opportunity and Affirmative Action Employer � M/F/D/V

For a listing of other career opportunities at ICF, please visit our Career Center at http://jobs.icfi.com

To Apply for this position, please CLICK HERE

Research Associate (Los Angeles, CA)

2009-10-14T22:04:04-07:00
Technical Services Associate - Los Angeles, CA 90039 Contract Assignment through end of April 2010

Summary:
Conduct biological, chemical and physical analyses on experimental materials (biologics and drugs) that support new product development, process and product improvements.

Essential Duties and Responsibilities:
1)Conduct critical biological, chemical and physical analyses on experimental materials that support product development, process and product improvement. Aid in the identification and technical assessment/evaluation of new technologies 2)Use sophisticated laboratory instrumentation and computer systems to collect and record data. Perform advanced assays requiring precise analytical skills and understanding of biology and chemistry principles.
3)Complete all testing, including special project / protocol testing in a timely and appropriate manner.
4)Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations.
5)Investigate deviations and write exception documents.
6)Participate in functions involving teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality.
7)Perform laboratory and manufacturing audits as required. Audit and update, as required, plant SOPs.
8)Perform equipment maintenance and calibrations as required.

Qualifications:
-Ability to handle multiple tasks concurrently, and in a timely fashion.
-Computer literate.
-Must be detail oriented, conscientious and have high reading comprehension skills.
-Must have basic understanding of laboratory instrumentation.
-Must be able to communicate effectively with supervisors and peers.

Education:
Bachelors Degree in Chemistry, or Biological Science with Analytical Chemistry or Laboratory coursework. Masters Degree preferred.

Physical Demands:
-Must be able to lift, push, pull and carry up to 50 lbs.
-In general, the position requires a combination of sedentary work, performing experiments at different locations and walking around observing conditions in the facility.

Working Environment:
-May have to work in controlled environments requiring special gowning. May be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet and body.
-May be working in a loud area that requires hearing protection and other protective equipment to be worn.
-Will work around chemicals such as alcohol, acids, buffers and celite that may require respiratory protection.
-May be required to work or be assigned to a different shift as needed.
-May be required to work in a confined area.
-Inside working conditions.
-May have to work in cold temperatures
-Some Clean Room and cool/hot storage conditions.
-1% travel.

.

RESPOND HERE! To respond immediately, access the online response form at: http://sh.webhire.com/servlet/resp/rf?jobid=2401123&boardid=1904

Have Year Round Allergies? Be in a Study & get Compensated

2009-10-14T16:27:04-07:00
Do you have allergies all round the year and manage them using over the counter medication as needed. You have a chance to be part of a research study with FDA approved medication and be compensated for time upto $925 for participation. It involves 11 visits to the doctor's office over a period of 27 weeks.

If you are interested please fill out the signup sheet at http://www.calallergy.com/trials_signupform_la.html
or call (310) 966 9050 extn # 1

Product Formulator (Torrance, CA)

2009-10-14T15:30:28-07:00
Dietary Supplement Manufacturer-Product Formulator

Paragon Laboratories, a leading contract manufacturer of Dietary Supplements, located in Torrance, CA, has an immediate opening for a Product Formulator of Dietary Supplements and Herbal Products.

Job Responsibilities:
� Formulation of dietary supplements, including tablets, two-piece capsules and powdered dosage forms.
� Position will interact with the Sales, Manufacturing and Purchasing Departments to assist in meeting the product formulation needs of our customers.
� This will include research of ingredients to develop novel products.
� Review existing formulations to see if there are opportunities for improvement.

Qualifications:
� Minimum 3 years experience in the formulation of dietary supplements and herbal products.
� Must have experience in the product formulation of tablets, two-piece capsules and powdered dosage forms.
� Must have an intimate understanding of all phases of the production process including granulation, compression, encapsulation and coating.
� Skills must also include trouble shooting formulation problems in production.
� Excellent communication (verbal and written) and organization skills.
� Must have excellent computer skills that include word processing and spread sheet use.
� The candidate must be self-motivated, with the ability to initiate and follow through on assignments.
� Must have a minimum of a Bachelor of Science degree in Chemistry or related life science.

Benefits:
� We offer competitive salaries, depending on skills and experience.
� Quality work environment.
� Excellent benefits including Health Insurance and 401K plan.
� Opportunity to grow.
� We are an Equal Opportunity Employer.

Regional Sales Representative - Skincare / Dermatology (Los Angeles Basin)

2009-10-13T21:30:06-07:00
Regional Sales Representative

Leading international skin care Products Company is expanding its U.S operations and is seeking seasoned sales representatives to lead their entry into key regions in the Los Angeles Area. Successful candidates will focus on utilizing effective selling techniques to deliver customer service which will include, but is not limited to, sampling, providing patient education materials, educating demonstrating sales ability/ persuasiveness to physicians and staff to deliver focused sales messaging to targeted customers. This person will be responsible to maintain productivity metrics and peer to peer engagement opportunities.

Responsibilities include:

� Providing advanced product knowledge to Physicians, Clinics, Hospitals, Spas and other operations within the medical community of the assigned region.
� Promote/sell the medical line of skin care and skin treatment products designed and produced by the company.
� Negotiate contracts, monitor results and optimize accordingly in order to generate high-quality, cost effective ROI.
� Developing long-lasting relationships and trust with clients.
� Focuses sales efforts by analyzing reports, DDD data, target list and appropriate territory information.
� Participating in sales meetings, conventions and training programs
� Shows persistence and seeks alternatives when obstacles arise; seeks alternative solutions; does things before being asked or forced to by events.
� Effectively managing a territory to insure achievement of sales goals
� Follow AMA guidelines regarding entertainment/gift to physicians.
� Maintain current, approved protocol and company promotional materials to be used in sales presentations.
� Maintain and monitor sample inventory with proper accountability and follow PDMA/FDA guidelines.
� Monitor competition by gathering current marketplace information on pricing, products, new products.
� Implementing marketing and sales strategies on daily basis

Qualifications:
� BA/BS from an accredited school required. Focus in business or life science preferred
� 3+ year�s pharmaceutical/medical sales with a documented track record of success required.
� Demonstrated ability to learn and apply technical and scientific product-related information
� Demonstrated ability to manage territory budget
� Valid driver's license with a clean driving record and ability to pass a complete background check
� Consistent track record of quantifiable/documented sales and leadership accomplishments
� Demonstrated ability to plan, analyze and act upon sales data within an assigned geography
� Solid business acumen including excellent and persuasive business communication
� Demonstrated ability to work independently and exercise good business judgment and discretion and to analyze and address territory opportunities by building key customer relationships
� Computer Skills: proficiency in business software (MS Outlook, Word, Excel)

Benefits:
� Competitive Base Salary + Commission.
� Medical and dental benefits package

Our recruiters at Talent Solution Partners are proud to be your guide through the extensive maze of your job search. We are a well regarded national recruiting firm because of the partnership we exhibit with both our candidates and clients. Our staff at Talent Solution Partners is dedicated to locating qualified applicants for companies selling pharmaceuticals, medical devices, capital equipment, and services.
We are seeking top-tier and highly qualified sales professionals to explore the many exceptional job opportunities within the markets we serve.
To initiate the process, please email us a current copy of your resume. Please ensure all relevant information is included, this will help our staff to expedite the contact process where appropriate. Emails can be sent to ccareaga@talentsolutionpartners.com. Also, please visit us at www.talentsolutionpartners.com.

PROJECT DIRECTOR (Los Angeles, CA)

2009-10-13T16:58:59-07:00
Qualifications: Masters degree or greater preferred. 5 or more years experience with research. 2 or more years experience with team management Outstanding leadership and organization skills, with a proven track record of successful project management Excellent skills in team building and management, written and oral communication, project management, and budget management. Bilingual Spanish and English strongly preferred

Function: As project director of the Alliance Health Project, the Director will be responsible for overseeing all day to day activities of the research project. This includes managing IRB submissions, organizing team meetings, keeping meeting notes, liaison with the survey research core, overseeing subject recruitment, oversight of RA productivity and accuracy in data collection. The Project Director will assist the Alliance in and LAUSD in finding, tracking and recruiting subjects and will assist in tracking subject recruitment and data collection. The Director will also lead or co-lead biweekly team meetings with the RA and survey research core staff. Finally, the Project Director will assist in manuscript and powerpoint presentations. The Project Director will also have to occasionally visit each data collection site.

Status: Full time

Salary: Negotiable depending on education and experience, minimum $55k

UCLA AA/EOE

QC R&D Chemist (Pomona, CA)

2009-10-12T15:38:36-07:00
Biophase Solutions specializes in placing the top talented professionals in the leading Biotechnology and Pharmaceutical Companies in Southern California. We are currently recruiting for a QC Chemist to work for a Pharmaceutical Company in Pomona, CA.

BS or MS in Chemistry

Must have 2+ years experience working in the Pharmaceutical industry and be familiar with FDA/ISO/GMP procedures.

Should be familiar with:
Gas/Liquid Chromatography
Mass Spectrometry
Ion Chromatography
Nuclear Magnetic Resonance
FT-IR Spectroscopy
UV-VIS Spectroscopy
Rheometry
Refractometry
Polarimetry
Thin Layer Chromatography
High Performance Liquid Chromatography
SDS-PAGE
Western Blot

Contract to Hire (3 months contract)
Salary up to 50K
Monday-Friday 8AM-4:30PM

Please send your resume to Chris@biophaseinc.com along with a brief cover letter explaining your qualifications