eBay Classifieds  » Jobs » Biotech, R&D, & science » 1-22 of 22 ads for biology in San Francisco Bay Area

Hello,   My name is Jim and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Research Associate for a prominent client of ours.  This position is located in South San Francisco. Details for the positions are as follows:   Job Description:   ·         We are seeking a Research Associate/Senior Research Associate in the Department of Safety Assessment for conducting and overseeing scientific investigations and screening activities to support discovery and ...

  Title: Sr. CRA Company: Pharmaceutical Location: San Francisco Role: • The Senior CRA is responsible for the implementation and management of assigned clinical studies, focusing on the areas of protocol development, study planning and conduct, site monitoring and/or monitoring management, enrollment and data quality, and adherence to corporate timelines and objectives. Responsibilities: • Ensures that clinical documents (i.e. protocols, ...

Associate Scientist II - R&D needed at biotech company for special project. Six month contract+, fulltime hours, $43.00/hour, W-2. **Please note the PhD requirement; candidates with MS degrees may be considered with at least 4+ yrs relevant experience.   Duties              Conduct routine scientific experiments using common laboratory equipment and calculations. Assist or on occasion drive the evaluation and procurement of equipment and materials. Understand the New Product Introduction process and ...

Duties • Candidate with experience in techniques that include rodent handling, health monitoring, blood and tissue collection, and dosing via multiple routes. Skills • 5-10 years of hands-on experience conducting studies using experimental rodent models. • Basic molecular biology skills required. • Must have strong written and verbal communication skills. • Must be proficient using Excel, Word and PowerPoint. • Must be a strong team player who quickly learns new in ...

Provide strategic leadership for teams focused on the development of personalized medicine based on the discovery of molecular biomarkers. Utilizing patient derived data from genomic and molecular analyses you will develop strategies to identify new therapeutic targets. Shall: *** Establish internal collaborations with preclinical research and clinical science develop pre clinical plans to validate new pathways associated with drug response and translate findings into clinical practice *** ...

Qtech-Sol Internship program develops technical skills and knowledge pertaining to roles and responsibility to be performed as Drug Safety Associates.   Before the internship the professional training is required, which provides real time experience and exercise learning pattern.   Educational Qualifications: Bachelor Degree or Higher in Life Science             Preferred degree in: Anatomy, Biochemistry, Biotechnology, Biology, Biomedical             Science, Biomedical Engineering, Chemistry, ...

 A small medical device company is looking for a Quality Control Laboratory Analyst. The position will be responsible for the coordinating of testing and review of all QC test data as well as assuring department compliance with Quality Systems documentation and regulatory requirements.     RESPONSIBILITIES INCLUDE: ·       Oversee the stability testing program ·       Oversee the calibration and preventative maintenance program for all QC equipment ·       Oversee the validation and analytical method ...

Major developer of novel renal therapeutics seeks Phd with thorough understanding of renal disease pathophysiology and detailed experience performing small animal handling and surgery to provide hands-on leadership in the design and execution of pharmacology experiments and in vivo studies to evaluate new renal therapeutic drug candidates. This includes, but is not limited to: developing and characterizing mouse models of kidney disease, running in vivo screening cascades to support lead ...

Seeking PhD, ability to design and conduct in vitro cell based assays, stem cell differentiation, and biochemical assays, and a history conducting muscle and biological fluid histological analysis to lead a team of scientific professionals performing: *** Development and execution of cell based assays to support mechanism of action and target validation studies. *** Biomarker discovery and translational studies to refine mechanistic understanding of molecular targets in chronic kidney disease. ...

Contact Jeff at 815-756-1221 for more details. Qualifications: - BS Food Science, Nutrition, Biology, Chemistry - 5+ years of product development, frozen food experience desired - Excellent communication and organizational skills - Strong technical skills - Ability to taste/ingest food products - Culinary skills, ability to formulate recipes and develop products from bench top to commercialization - US Citizen/Perm Resident Job Scope: - Will be responsible for developing new food products - ...

Hello,   My name is Chris and I represent The Fountain Group.  We are a national staffing firm and are currently seeking an Associate Scientist II for a prominent client of ours.  This position is located in Emeryville, CA. Details for the positions are as follows:   Job Description Job Title :   Scientific Associate II Duties  Candidate with experience in techniques that include rodent handling health monitoring, blood and tissue collection, and dosing via multiple routes. Skills 5-10 years of hands ...

My name is Jessica, and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a  QC Lead Compliance Reviewer for a prominent client of ours.  This position is located Emeryville, CA. Details for the positions are as follows:   Job Description/Requirements: Duties              Provides timely and accurate technical and compliance review of test records generated in cGMP testing on hard copy test records and/or in the computerized LIMS database for release, ...

Seeking leader with 10+ years in pre-clinical drug discovery and Ph.D. in cellular or molecular immunology or MD with training in respiratory, inflammation or autoimmune disorders and a track record of successfully moving drug leads through discovery process to clinical phase. Requirements: *** Track record managing operational budgets. *** Ability to recruit, lead and develop top rated scientists in a multi-task extremely fast-paced environment and constantly changing priorities. *** ...

Seeking a proven leader with experience leading preclinical research of novel protein therapeutics for autoimmune diseases. Shall manage the following activities: *** Target discovery, translational research, biomarker assay development, mechanism-of-action studies, In Vitro and In Vivo models *** Establishing and managing strategic collaborations with pharmaceutical and academic organizations *** Supervising up to 10 scientists Candidate must possess 10+ years of experience and PhD in ...

To develop and improve analytical testing methods for microbially produced diagnostic antigen products and to assist in method transfers to QC. Assist in development of state of the art analytical methods for testing of protein antigen products that reliably and reproducibly meet Novartis Diagnostics business requirements Assist in the implementation of new analytical technologies and improvement of existing technologies in the group Prepare and review scientific experiment protocols and reports ...

 Manufacturing Technician III, Bulk Fill and Label Center The Manufacturing Technician III performs fill operation of 24+ antigens and 7+ peptides, including preparation activities such as material cleaning, autoclaving, depyrogenation, visual inspection, label issuance and reconciliation, label application and packaging. The Technician III is expected to perform operations under cGMP/ISO/FDA guidelines, follow valid procedures and documentation and work with other Bulk Fill-Label Center team ...

Manufacturing Associate III, Bulk Fill and Label Center The Bulk Fill-Label Center Associate III performs fill operation of 24+ antigens and 7+ peptides, including preparation activities such as material cleaning, autoclaving, depyrogenation, visual inspection, label issuance and reconciliation, label application and packaging. The Associate III is expected to perform operations under cGMP/ISO/FDA guidelines, follow valid procedures and documentation and work with other Bulk Fill-Label Center team ...

 Data Analyst/Programmer .  •Support a KPI reporting system to provide the business with meaningful metrics that will drive continuous improvement •Ensure that any updates to data that are required to bring a source system into compliance is communicated to the source system owner •Establish a sound working relationship with source system owners (including Logistics Service Provider systems), business process owners and technical experts •Ensure that data set up processes follow GMP compliance ...

Responsibilities: • Develop and improve analytical testing methods for microbially produced diagnostic antigen products and to assist in method transfers to QC. • Assist in development of state of the art analytical methods for testing of protein antigen products that reliably and reproducibly meet client’s business requirements • Assist in the implementation of new analytical technologies and improvement of existing technologies in the group • Prepare and review scientific experiment protocols ...

Responsibilities: Duties: • Performs the review of QC Microbiology Test Record documentation for accuracy and completeness according to cGMP’s to ensure timely release of product or facility/utility. • Performs and completes review of QC Microbiology test results in the laboratory information management system (LIMS). • Compiles and transfers completed records to customers, including Quality Assurance, Quality Control, and Validation, maintaining chain of custody. • Adheres to internal/external ...

Seeking scientist with 5+ years invitro assay development experience to provide molecular pharmacological properties related development and expert support to teams developing optimal therapeutic efficacy of GPCR modulators. Requires: *** PhD in biochemistry, cell biology or molecular biology or simial and 3+ years Postdoc experience. *** Knowledge of GPCR pharmacology. *** Hands-on radioligand binding assays, second messenger signaling assays, confocal microscopy, bioluminescence, Forster ...

Licensed Clinical Laboratory Scientist (CLS) General Supervisor Description: The Clinical Laboratory Scientist General Supervisor is responsible for supervising Clinical Laboratory Scientists and Clinical Lab Assistants, performing high complexity laboratory testing on patient specimens, interpreting and reporting patient results, performing quality control and quality assurance procedures, and complying with all applicable local, state and federal laboratory ...