Quality control Supervisor
: Job Details :


Quality control Supervisor

gonzer

Location: West Nyack,NY, USA

Date: 2024-11-07T08:32:10Z

Job Description:
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
Apply Now!

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