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The individual will assist in the development, implementation and maintenance of quality control systems and laboratory activities to insure compliance with regulatory requirements.


• Responsible for conducting routine and non-routine analysis of raw materials, in process, and finished formulations according to standard operating procedures.
• Compiles data for documentation of test procedures and prepares reports.
• Reviews data obtained for compliance to specifications and reports abnormalities.
• Revises and updates standard operating procedures as needed.
• Applies knowledge of good manufacturing practices and good laboratory practices on a daily basis.
• May provide guidance to other lower-level personnel.
• Develop, validate/qualify, and improve assays for better efficiency and consistent results.
• Review QC test results to ensure that specifications are met and that testing has been performed according to cGMP and GLP requirements. Make recommendations for any corrective actions.
• Ensure on a daily basis that the laboratories are in cGMP compliance.

• BS degree, MS preferred, in Molecular Biology, Cell Biology, or Biochemistry
• Minimum 5 years biotech/pharmaceutical experience in quality control or molecular biology.
• Must have experience with the documentation and implementation of quality control systems in a biotech/pharmaceutical setting.
• Prefer experience in cell culture.
• Must have experience in molecular biology.
• Must have strong computer skills; Microsoft products.
• Must be able to communicate intelligently with co-workers.
• Must have initiative, high attention to detail, and the ability to multi-task.

We offer a competitive compensation package along with outstanding benefits. For confidential consideration, please a resume with a cover letter and salary history.

Argos Therapeutics is an Equal Opportunity Employer.