QA Specialist

Proclinical is currently recruiting for a QA Specialist with a pharmaceutical company located in Burlington, MA.

Job Responsibilities:

• Provide support to the cGMP compliance function.
• Responsible for the processing, formatting, obtaining approvals, mastering, distribution and archival of Standard Operating Procedures, Forms, Batch Records, Protocols, Material Specifications.
• Send GMP documents to the clients for their review and approval.

Skills and Requirements:

• Demonstrates basic knowledge of current Good Manufacturing Practices (GMPs) and/or Good Laboratory Practices (GLPs).

• Strong organizational and attention to detail.
• Strong verbal and written communication skills and interpersonal skills.

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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