Associate Scientist I – 6 month contract
To perform laboratory-based Analytical testing by executing release testing methods (QC). To provide results for MS&T Fermentation and Purification studies or to provide support of QC or Manufacturing deviations investigations. Ensure the Analytical laboratory equipment, reagents and chemicals are stocked and ready to perform testing according to the Analytical laboratory schedule.
Working under moderate to high degree of supervision from Lab Manager and ...
CONTRACT / 7-9 MONTHS..COULD BE EXTENDED..GREAT OPPORTUNITY
High school diploma (or GED equivalent) and some college coursework in the biological sciences (including laboratory coursework). A certificate in Biotechnology, Associate degree in Biology or Chemistry is preferred. Related experience may substitute for education.
Specific functional responsibilities:
-Production Planning/Execution –
-Work with the team member and area lead to complete schedule for cleaning/autoclaving ...
Responsible for implementing set-up, execution, oversight and reporting of clinical studies while ensuring that the conduct of the trial is in compliance with the protocol, ICH/GCP, and applicable regulatory requirements.
Key Accountabilities/Core Job Responsibilities:
Lead multifunctional team through clinical studies activities that meet ICH/GCP and SOP requirements
Develop clinical trial protocol synopsis, protocols, amendments and informed consent documents
Must have strong written and verbal skills.
Must be able to work in a team-oriented environment.
Must be creative, highly organized, self-motivated, perceptive, and innovative.
Must have strong analytical and decision making skills. Able to make decisions with limited supervision.
Technical skills requirements
Must have experience in GMP manufacturing.
Must have experience in FDA and ISO regulated environments.
Must have adequate knowledge of reagent preparation ...
Position: Major Tasks
Provide expert leadership in medical device regulations in an individual contributor role including: the ability to identify issues of significance, communicate complex issues to site leadership, provide multiple alternatives to the solution of complex problems and the ability to provide guidance in their implementation.
Leads relevant medical device project planning and review meetings; communicating to senior leadership regarding program status and supporting final ...
Perform scaled down purification studies to support the development of new processes or to improve the existing manufacturing processes in addition to providing support for QC or Manufacturing deviations investigations.
Working under moderate to high degree of supervision from Lab Manager and/or senior Associates II.
Executing scientific protocols in a team setting using scaled down column chromatography operations and ultra/dia-filtration.
Ensuring their own experimental ...
Global Product Strategy, the department to which this position belongs to, provides strategic business direction from research through to development, commercialization and medical excellence, collaborating with functions and affiliates to shape the future of medicine. The Strategic Insights & Analysis Team provides high quality insights on the brand(s) and the market environment for the relevant disease area based on market research, publicly available brand and market information, and non-publicly ...
B.Sc./M.Sc. in Chemistry/Biochemistry or related discipline
1 to 5+ years of experience in either an Analytical Development or QC Testing environment in the biotechnology or diagnostics industry
Prior experience working on Analytical testing of recombinant proteins.
Working under moderate to high degree of supervision on Analytical testing using up to 2 different methods
Experience maintaining laboratory scale Analytical equipment
Good verbal communication skills
Potential for ...
To perform routine laboratory-based Analytical testing for product release.
Ensure the Analytical laboratory equipment, reagents and chemicals are stocked and ready to perform testing according to the Analytical laboratory schedule (80%).
Independently perform studies with complex scope with some supervision from the Lab Manager to support purification process characterization, process improvement or investigation of purification process-related deviations using ...
Oversees Clinical Data Management processes, ensuring timelines and contracts are adhered to and quality standards are met. Maintains system validation documentation and other regulatory documentation. Manages, monitors and reports on progress of Data Management projects. Responsible for resources planning and tasks assignment of direct reports. Supports department infrastructure. Supports department head by successfully completing ad hoc projects to improve departmental ...
Clinical Research Associate - San Francisco Office
Immune Design is leveraging two powerful, versatile discovery platforms of innovative technologies that work in partnership to develop product candidates that activate, guide, and strengthen patient-specific immune responses to potentially fight cancer and other chronic diseases. The Company was founded in 2008 with cutting edge molecular tools to shape the immune response by selectively activating and targeting dendritic cells. ...
Associate Director QU Process Validation
Responsible for strategic leadership and oversight in the development and maintenance of the Process Validation program for the Supply Center and for aligning process validation standards with global production sites. Directs process validation life-cycle program and defines required activities to maintain facilities, utilities, technical systems and bio-pharmaceutical manufacturing processes associated with new, modified, or existing facilities ...
Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.
Title: Environmental Health & Safety (EH&S) Associate II
Job ID: 23438
Location: South San Francisco, CA
Duration: 6 Month Contract
Pay Rate Range: Depends on Experience (W-2 all inclusive rate)
Will provide technical support to ...
Mar 6 -
South San Francisco
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