QA Specialist

Highly Competitive Salary
  1. Permanent
  2. Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), Good Clinical Practice (GCP)
  3. United States
Burlington, USA
Posting date: 28 Jul 2020
This vacancy has now expired

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.