QA Manager

The Wellington Group has been engaged to find an experienced QA Manager who will be responsible for site wide QA compliance in a cGMP environment.  Put your QA Management experience to work in a new job today!

Position Duties:

  • Lead and manage all site quality assurance operations in order to assure the quality of raw materials from suppliers, work in process and finished product manufactured at the facility
  • Serve as primary site contact for regulatory, customer or third party audits
  • Formulate responses to any findings from the audit and issue corrective actions where needed
  • Develop and execute site QA operating budget and manage department efforts to control costs within approved levels
  • Develop direct reports and work closely with them to ensure that a consistent approach is taken in evaluation of quality issues
  • Collaborate with operations management team to develop projects to align with the strategic vision of the facility and support key performance indicators

The qualified candidate will have:

  • BS Degree in life sciences, MS or PhD
  • 7 to 10 years experience in Quality Assurance, including a minimum of 3 years supervising and managing staff
  • Strong background in chemistry and/or microbiology is preferred
  • Experience with CAPA, OOS and Audit finding is required
  • ASQ Certifications preferred
  • Prior work experience in a leadership role in a GMP or FDA regulated manufacturing facility (cosmetics, drugs, devices or food)
  • Strong verbal, written, analytical and interpersonal skills
  • Ability to organize and prioritize workload and to meet deadlines

Industry: QA Manager, FDA, cGMP, ASQ, Audits, CAPA, Regulatory

Job Code: 445-32-MH2322

Location: New York, no relocation

Apply directly at:

Don’t wait, apply with The Wellington Group today!
(all information will be held in the strictest of confidence)

The Wellington Group (   910-338-2795

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