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Job type: Permanent

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

Location: United States

Proclinical is currently recruiting for a QA Specialist with a pharmaceutical company located in Grand Rapids, MI.

Job Responsibilities:

Support the effective and compliant execution of tech transfer activities and development of necessary quality systems at the manufacturing sites and associated off-site storage locations.
Support site qualification activities and development of quality agreements in accordance with company standards.
Perform review and approval of equiptment and facility qualifications, technical documents, raw material specifications, analytical methods, and master batch records to ensure company products/processes comply with cGMP requirements.

Skills and Requirements:

Bachelor's Degree with a concentration in science, or an equivalent technical discipline.
Minimum of 8 years working in an FDA regulated environment.
Experience in pharmaceutical aseptic manufacturing operations and quality assurance.
Detailed knowledge of cGMPs related to pharmaceutical production.

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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