Quality Control Manager - Synerfac : Job Details

Quality Control Manager

Synerfac

Job Location : West Nyack,NY, USA

Posted on : 2024-09-21T06:36:25Z

Job Description :

The Quality Control Manager is responsible for all aspects of Quality measurement, product inspection and in-process testing in West Nyack, NY. The primary responsibility is to ensure that Quality Control personnel perform the required inspection accurately and as specified by the appropriate quality documentation. This position will allocate resources to efficiently maintain orders on schedule. The Quality Control Manager is responsible for the training, the discipline and morale of the staff and will report to the VP of Quality/Reporting. Essential Functions•Quality Control - Product Inspection and Releaseo Testing of materials required to produce a finished product and the final product to confirm compliance to issued specifications. •QC Inspectors are responsible for (but not limited to)* Physical - Dimensions, Hardness, Drop test, tap test, net weight; Visual - Color (e.g. color matching), Appearance; Sensory - Odor, Textureo Product Disposition•Determine final disposition of all products•Responsible for approving and rejecting all batches•Management of Product Hold and Dispositiono Quality Control Documentation/Samples for Clients•Conversion of Product Specifications to Production Line Documentation (checklists, forms)•Finished Product Documentation to be issued to Clients, (e.g. COA)•Pre-Shipment Samples to Clientso Management of Documents and Product Samples Retention Requirements•Records /Documentation review and sign off for OTC Productso Monitor and Confirm production operations conforming to specifications or requirements•Line Clearance•Critical Process Parameter Line Set Up•Management of Staff•Manage QC work schedules; accountable for QC team s work hours•Responsible for allocating QC personnel to the production line•Perform staff performance evaluationJob RequirementsJob Qualifications•Bachelor s degree in Applied Sciences or Engineering (e.g., Biology, Chemistry, Physics, or a related field).•At least 5 years of experience in Quality Management, QA, or QC.•Proven expertise in Quality Management.•Familiarity with Quality Systems, including GMP and GLP, in an FDA-regulated industry.•Strong critical thinking and problem-solving skills, with the ability to identify and resolve issues promptly, analyze information effectively, and develop alternative solutions.•Excellent interpersonal and communication skills.•Capable of managing and developing staff.•Collaborative team player.•Self-motivated and proactive.

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