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Job ID: 4503
Employer: SRI International
Position: Supervisor - Analytical Chemistry
Description: The Supervisor will provide analytical expertise and leadership supporting nonclinical safety studies conducted under Good Laboratory Practice regulations. The Supervisor will collaborate closely with other nonclinical development team members including formulation development, dose preparation, toxicology, pharmacokinetics, project management, and quality assurance.
The Supervisor will be asked to:
- Provide input in analytical method development, verification, validation, analysis of data, research techniques, and problem solving.
- Monitor the generation of analytical data, ensure appropriate and current test methods are used, and critically evaluate the validity of results.
- Write reports and respond to QA audits of raw data and reports.
- Supervise GLP analytical chemistry services and staff, write and review proposals and protocols, develop budgets for project tasks.
- Ensure adherence to SRI policies and quality programs.
Requirements: PhD and >5 years experience in chemistry or equivalent with coursework in Analytical Chemistry. Experience with GLP and/or cGMP regulations and supervisory experience desirable. Excellent oral and written communication and interpersonal skills and ability to work in fast paced team environment.
Post-offer, pre-laboratory physical examination will be required.
About SRI:
SRI International is a leader in the development of new products for the treatment and diagnosis of disease, primarily in the areas of cancer, infectious disease, neuroscience, and immunology. SRI's Biosciences Division works in several ways, conducting basic research like an academic institution, performing drug discovery and biologic development like a biotechnology company, and carrying out preclinical development and pharmaceutical services like a contract research organization - from "Idea to IND" (tm).
The Biosciences Division works with partners and clients on a broad range of preclinical discovery and development projects, utilizing its expertise in medicinal chemistry, custom organic synthesis, efficacy pharmacology and safety evaluation, pharmacokinetics and metabolism studies, analytical chemistry, formulation design, drug product manufacturing, project management and regulatory affairs. Many studies are conducted under FDA's GLP and GMP regulations. SRI currently has several drugs on the market, several more in clinical trials, half a dozen in preclinical development, and has assisted in the development of more than 130 other products that made it to clinical trials or reached the market.
Location: Menlo Park, CA
Contact: Apply via our web page www.sri.com/jobs to job number 100559.
Post Date: 8/23/2010 9:30:06 AM
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