Our pharmaceutical client is seeking a Quality Control Supervisor to lead their QC team to ensure compliance with regulatory standards. If you are looking for a company that values leadership & growth, we'd love to hear from you.
Responsibilities:
- Maintain laboratory instrumentation, including equipment qualification, and preventative maintenance programs. May need to assist with troubleshooting and minor repairs.
- Support training and troubleshooting efforts for staff.
- As necessary, review completed laboratory testing to support the timely release of data, reports, and material.
- Coordinate and oversee the status of offsite sample testing.
- Maintain and manage cGMP and general lab systems at defined levels of compliance.
- Draft and review various documents in support of laboratory efforts and production campaigns.
- Maintain laboratory systems and documentation.
- On a rotating coverage, provide laboratory on-call support coverage for all aspects of laboratory operation, including environmental testing, raw material testing, in-process testing, isolated intermediate testing, and finished good product release.
- Work cross-functionally with other departments (such as Operations/Production) to ensure deliverables are met according to projected timelines.
- Verify timecards and SAP billing is completed accurately and on time as per the site-specific timelines.
- Perform the QC release for raw materials, isolated intermediates, and finished goods.
- Identify discrepancies, author out of specification and deviation investigations within TrackWise, and implement associated CAPAs.
Qualifications:
- Bachelor's Degree in Chemistry, Pharmacy or closely related field required. Advanced degree highly beneficial.
- 5 or more years of experience in manufacturing support laboratory in the pharmaceutical industry
- Management of 24/7 lab operation highly beneficial
- Hours: 7pm - 7am