| Company: | GenQuest BioScience, Inc. |
|---|---|
| Type: | Contract |
| City: | Mountain View |
The selected candidate will perform daily QC testing activities to support the development and manufacture of drug/device products. Write and implement QC protocols for test method qualification/validation, and other quality processes as needed. Train QC analysts on quality procedures. Deliver timely, accurate and reliable sample testing results following standard operating procedures in a cGMP laboratory to support product development and release of clinical and commercial materials and product. Primary analytical techniques are HPLC, GC, UV, FT-IR, and other wet-chemistry related tests. Conduct routine and non-routine analysis of raw materials, in process, and finished formulations according to standard operating procedures. Conduct thorough laboratory investigations and generate corresponding report. Identify CAPA and ensure follow-up for closure. Compile data for documentation of test data and prepare reports. Review QC data for compliance to procedures and specifications and report abnormalities. Refine testing methods and compile data for documentation of test procedures as needed. Revise and update standard operating procedures as needed. Pursue and resolve analytical and instrument issues. Apply knowledge of Good Manufacturing Practices and Good Laboratory Practices on a daily basis.
Qualifications include a BS/MS degree in a scientific discipline 5-8 years experience in a cGMP quality control laboratory. Analytical method validation experience preferred. Experience with USP testing methods a plus. Prior experience in device development or pharmaceutical environment preferred. Must be highly organized, detail oriented and able to manage multiple projects. Ideal candidate will have laboratory skills that include computer controlled HPLC, GC, UV, IR, workstation software, office software (MS Excel, MS Word, etc) and compliance level record keeping. Solid communication and presentation skills required Supervising experience preferred. Prior experience in device development or pharmaceutical environment preferred. Please note that this is a project specific position on contract for approximately four months in duration.
How to Apply:
Resumes must be sent via e-mail only and as a file attachment in either MS Word or Rich Text format to: jobs@genquestbio.com
To learn more about this position or to preview other opportunities, please visit our website at:
www.genquestbio.com/careers.htm
Follow us on Twitter:
www.twitter.com/GenQuestBio
Qualifications include a BS/MS degree in a scientific discipline 5-8 years experience in a cGMP quality control laboratory. Analytical method validation experience preferred. Experience with USP testing methods a plus. Prior experience in device development or pharmaceutical environment preferred. Must be highly organized, detail oriented and able to manage multiple projects. Ideal candidate will have laboratory skills that include computer controlled HPLC, GC, UV, IR, workstation software, office software (MS Excel, MS Word, etc) and compliance level record keeping. Solid communication and presentation skills required Supervising experience preferred. Prior experience in device development or pharmaceutical environment preferred. Please note that this is a project specific position on contract for approximately four months in duration.
How to Apply:
Resumes must be sent via e-mail only and as a file attachment in either MS Word or Rich Text format to: jobs@genquestbio.com
To learn more about this position or to preview other opportunities, please visit our website at:
www.genquestbio.com/careers.htm
Follow us on Twitter:
www.twitter.com/GenQuestBio
