Quality Manager III
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The Opportunity
Description
We're looking for a Quality Manager III, working in Pharmaceuticals and Medical Products industry in 1000 Research Parkway, Meriden, Connecticut, 06450, United States.- Responsible for Vendor and Supplier Management
- Responsible for Supplier Quality
- Responsible for Auditing cGMP
Our Client
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
- Bachelors degree in engineering or technical discipline (Master degree prefered)
- Experience in pharmaceutical/biopharmaceutical industry or related industry/cGMP environment
- Ability to work on strict deadlines
- Background in life science
- Ability to interface with cross-functional teams
- Detail oriented
- Strong working knowledge of the FDA Quality System Regulation
- Experience leading CAPA (Corrective and Preventive Action) activities
- Ability to handle multiple projects concurrently
- Well-developed communication skills, both verbal and written
- Experience in vendor/supplier management quality systems and auditing techniques
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?
Apply Now
