QA Specialist job in La Verne, USA

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Job type: Permanent

Discipline: Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP)

Location: United States

This vacancy has now expired. Please see similar roles below...

Proclinical is currently recruiting for a QA Specialist with a pharmaceutical company located in La Verne, CA.

Job Responsibilities:

Responsible for QA documentation review of validation protocols and final reports as well as any other Validation/Engineering documents which are project related.
Required to provide quality oversight to Validation, Engineering and Manufacturing in order to ensure compliance of documentation

Skills and Requirements:

Candidate must demonstrate a strong knowledge of Validation and Aseptic Manufacturing principles.
Understanding of Manufacturing process equipment such as autoclaves, lyophilizers and isolators is preferred.

If you are having difficulty in applying or if you have any questions, please contact Catherine Nguyen at 215-531-5643.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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