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Job type: Permanent

Discipline: Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Pharmacovigilance Practice (GVP)

Location: United States

Proclinical is currently recruiting for a QA Associate with a pharmaceutical company located in Cambridge, MA.

Job Responsibilities:

Review of event documentation such as Batch records, Exceptions, and Regulatory filings
Production record review and Product disposition for drug substance, drug product, device assembly and finished goods
Support design development plan including design verification and DHF deliverables
Build and maintain Product Specification Files (PSF) for company program

Skills and Requirements:

Minimum, a BS degree in life sciences, engineering or related field
Minimum of 5 years pharmaceutical quality assurance experience in a GMP manufacturing and supply chain environment
To have been involved on a device development project before as QA
Signed off on design development plan, completed design verification, approved DHF deliverables

If you are having difficulty in applying or if you have any questions, please contact Janelle Jones at 617-830-7544.

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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