Quality control Supervisor - gonzer : Job Details

Details: L.J Gonzer Associates is looking for individuals to join our pool of qualified candidates for potential assignment as a 2nd shift Quality Control Supervisor with our client based in West Nyack, NY. You'll be responsible for product inspection and in process testing.

• Managing and maintaining the retain room for samples and batch records storage and retrieval. Following up on sample/record requests verbally, manually or via email
• Ensuring adequate QC inspector coverage for Mon-Sat. Working overtime and adjusting to production demands and schedule as needed
• Ensuring all inspections, paperwork and sample collections are performed completely, accurately and timely
• Coaching, counselling and correcting the QC inspectors as necessary. Providing training, instructions and corrective action
• Reporting problems, issuing non-conforming reports and recommendations where needed
• Guiding and enforcing all cGMPs for all shift personnel: gowning, eating/drinking, cafe, locker rooms, production, documentation, lot coding, housekeeping and C&S
• Assisting with investigations from respective shift
• Attending meetings/conference calls with or on behalf of, the QC Inspection manager
• Providing daily shift summary report via email to site management
• Generating and analyzing metrics obtained from the QC Inspection department for inclusion in QA reports
• Assisting with site wide GMP training as it pertains to QC Inspection
• Timely escalation of QC Inspection issues to QC/QA management
• Has the authority to make and execute decisions related to the production lines

Job RequirementsDetails:

• Bachelor's degree in Applied Sciences or Engineering (Biology, Chemistry, Physics, or a related field)
• 5 to 8 years of experience in Quality Control (QC) or Quality Assurance (QA) supervision
• Proven supervisory/management experience
• Supplier quality experience preferred
• Proficient in Quality Systems, including Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) in FDA-regulated industries
• Strong problem-solving abilities: Identifies and resolves issues promptly, gathers and analyzes information effectively, and develops alternative solutions
• Excellent interpersonal and communication skills, with the ability to engage effectively with internal and external clients
• Strong leadership and process improvement skills
• Adept at deviation management and investigation
• Team-oriented and self-motivated