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: http://www.maxhire.net/cp/?E55E65361D43515B7D52182B77501A6F482D7D
Don’t wait, apply with The Wellington Group today!
(all information will be held in the strictest of confidence)
The Wellington Group ( https://twgrecruiters.com) 910-338-2795