Location: West Nyack,NY, USA
The Quality Control Supervisor is responsible for product inspection and in process testing. The primary responsibility is to ensure that Quality Control personnel (QC inspectors) perform the required inspection accurately and as specified by the appropriate quality documentation. This position reports into the Quality Manager and is located in Congers, NY. Essential Functions•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.3PM - 11PMJob RequirementsJob Qualifications•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