QA Associate

Highly Competitive Salary
  1. Permanent
  2. Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP)
  3. United States
Durham, USA
Posting date: 05 Jan 2021
This vacancy has now expired

Proclinical is currently recruiting for a QA Associate with a biotechnology company located in Durham, NC.

Job Responsibilities:

  • Issuance of Batch Production Records, Solution Lot Records, Labels, and Logbooks.
  • Review and approve site-specific GMP documents and records. This includes, but is not limited to, document creation, revision, review, change control guidance/review/approval, document issuance oversight, and document maintenance.
  • Contribute to oversight of quality systems and GMP activities, as well as site performance monitoring systems.
  • Identify and implement Quality System improvements.
  • Develop and support training on basic GxP quality systems.
  • Prepare for and support site inspections and audits.
  • Review changes to existing Quality Systems and GMP processes, identify gaps in existing Quality systems and propose solutions to site management.
  • Gain knowledge and understanding of quality systems, contribute to oversight of quality systems, and maintain GMP activities at the facility.
  • And other job duties that may be assigned from time to time.

Skills and Requirements:

  • Bachelor of Bachelor of Arts/Science Degree in Life Science or other technical discipline preferred with 0-2 years related experience.

If you are having difficulty in applying or if you have any questions, please contact Jarred Fetterman at 215-531-5593.

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.