QA Specialist job in Burlington, USA

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Job type: Permanent

Discipline: Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), Good Clinical Practice (GCP)

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 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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