| Company: | GenQuest BioScience, Inc. |
|---|---|
| Type: | Contract |
| City: | Mountain View |
The selected candidate will perform daily QC testing activities to support the development, manufacture and release of drug/device products. You will deliver timely, accurate and reliable sample testing results following standard operating procedures in a cGMP laboratory. Perform primary analytical techniques of HPLC, GC, GC/MS, UV, FT-IR, and other wet-chemistry related tests. Conduct routine analysis of raw materials, in process, and finished formulations according to standard operating procedures. Compile data for documentation of results and prepare compliant reports accordingly. Conduct laboratory investigations on aberrant results when obtained. Work on special projects according to established protocols with minimum supervision. Apply knowledge of Good Manufacturing Practices and Good Laboratory Practices on a daily basis.
Qualifications include a BS degree in chemistry or a closely related scientific discipline with 8-10 years experience in a cGMP quality control laboratory. Analytical method validation experience a plus. Experience working in a matrix managed team environment and an ability to work effectively with all departments within the company. Experience with USP testing methods a plus. Prior experience in device development or pharmaceutical environment preferred. You must be highly organized, detailed oriented and able to manage multiple tasks concurrently. The 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. You will possess good laboratory skills in basic wet chemistry techniques and advanced testing applications. Work in a team environment and independently, if required. Solid communication and presentation skills required.
We also have a similar position open for a qualified candidate with 5-8 years of industry experience. Please note that this position is a project specific contract to last until mid November2011.
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, follow us on Twitter or to preview other opportunities, please visit our website at: www.genquestbio.com/careers.htm
Qualifications include a BS degree in chemistry or a closely related scientific discipline with 8-10 years experience in a cGMP quality control laboratory. Analytical method validation experience a plus. Experience working in a matrix managed team environment and an ability to work effectively with all departments within the company. Experience with USP testing methods a plus. Prior experience in device development or pharmaceutical environment preferred. You must be highly organized, detailed oriented and able to manage multiple tasks concurrently. The 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. You will possess good laboratory skills in basic wet chemistry techniques and advanced testing applications. Work in a team environment and independently, if required. Solid communication and presentation skills required.
We also have a similar position open for a qualified candidate with 5-8 years of industry experience. Please note that this position is a project specific contract to last until mid November2011.
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, follow us on Twitter or to preview other opportunities, please visit our website at: www.genquestbio.com/careers.htm
