Quality Assurance Manager ( GMP )

  • Confidential
  • North Chicago, Illinois
  • 6 hours ago
  • Full Time

Job Summary


Employment Type
Full Time
Salary
$110,000 - $120,000 Annual

Job Description


Quality Assurance Manager 

 

  • Perform and/or arrange QA/QC audits of the facility.
  • Successfully maintain all ISO and FDA accreditations and certifications.
  • Maintain plant regulatory compliance, including FDA, ISO, EPA, AIB, OSHA requirements, and facility/product registrations.

 

Are you looking to make a career change to a rapidly growing company? This exciting opportunity offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance and paid PTO. Does this position match your future career goals? Then this opportunity could be the right fit for you

 

Why should you apply for Quality Assurance Manager (Pharmaceutical) position?

 

  • A positive workplace culture
  • Competitive Salary
  • Career Advancement opportunities
  • Financial Growth

 

Responsible for overseeing the Quality Assurance Department and Analytical Lab, ensuring compliance with industry standards and regulatory requirements. Leads a team of three or more direct reports, managing quality control processes and driving continuous improvement in product integrity.

 

Education and Experience Requirements:

  • Bachelor's degree in Science
  • Internal and External auditing.
  • Successfully maintain all ISO and FDA accreditations and certifications.
  • Perform batch record reviews and manage product disposition tasks as needed.
  • Analyze and review deviations, complaint investigations, and change controls.
  • Maintain plant regulatory compliance, including FDA, ISO, EPA, AIB, OSHA requirements, and facility/product registrations.
  • Oversee preparation of and approval for all company SOP’s.
  • Update, draft, or review Standard Operating Procedures (SOPs).
  • Assist with reviewing supporting documentation to ensure accuracy.
  • Oversee the entire vendor management process to ensure efficiency and compliance.
  • Maintain and update the Vendor List and Approved Vendor List regularly.
  • Review and approve audit reports submitted by third-party auditors.
  • Strong computer skills, including MS Office (Word, Excel, PowerPoint.
  • Strong knowledge of global regulations for commercial & clinical operations.

Job ID: 476226953

Originally Posted on: 5/8/2025