QA Specialist

Highly Competitive Salary
  1. Permanent
  2. Good Manufacturing Practice (GMP), Good Pharmacovigilance Practice (GVP)
  3. United States
Grand Rapids, USA
Posting date: 22 Sep 2020

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.