Overview
Quality Control Supervisor (Quality) Jobs in Totowa, NJ at Englewood Lab
Title: Quality Control Supervisor (Quality)
Company: Englewood Lab
Location: Totowa, NJ
Title: Quality Control Supervisor
Reports to: QC Manager or Director of Quality
Department: Quality Control
Responsibilities:
Scheduling of QC Inspectors to one of the following areas: (i) Bulk Mfg with Review of In-process Batch Records and related documentation and Special Sample handling, OR (ii) Production areas/Assembly lines, Warehouse FG auditing, Special Sample handling, Review of In-process Fill/Assembly Records and related documentation
Conduct non conformance, product complaints, out-of-specification investigation and provide corrective and preventive actions with follow-ups within specified area(s)
Trains and supervises document review personnel; batch release personnel, issues certificates of conformance (COC), certificates of manufacture (COM), and certificates of analysis (COA) to customers on finished goods. Maintains accurate record of approved, quarantined, rejected products within specified area(s)
Ensure compliance to all SOPs and other regulatory requirements (e.g. FDA, EPA, OSHA, ISO 13485:2003)
Reviews finished goods with shipping department for formal FGs release and compliance to customer requirements
Work closely with Quality Assurance/Quality Systems Dept on all aspects of Quality and Compliance
Maintains a working knowledge of QC inspection requirements for components, raw materials, in-process/bulk and finished goods
Ensures that review of in-process activities in Manufacturing or Production/Assembly areas is conducted by QC inspectors for conformance to specifications; follow up on out-of-specifications including non conformances
Participates in In-process Quality in-house and outside training program
Conducts periodic analysis of In-process Inspection program and makes recommendations
Assist in interpreting and/or developing of customer specifications and requirements for assembly/packaging specifications
Assists in establishing production and assembly inspection information sheets and documentation as required
Maintains and updates ERP System, maintains repository of batch records/documents, and other Mfg & Assembly in-process Specifications
Reviews of batch records, work sheets, and Inspection documentation for completeness and correctness
Conduct non-conformance resolutions, complaint investigations, and associated corrective and preventative actions
Reviews of QC Inspection reports daily for correctness and completeness
Facilitates on site customer inspections, coordinating availability of product and communication of disposition to Quality and Inventory Control. Interfaces with customer distribution operations where needed
Maintains awareness and compliance with safety regulations in performing job duties
Reviews Production and in-process related information on batch records/documents
Ensure that finished goods, bulk, raw materials, components are maintained correctly in the warehouse and other holding areas
Assist in the review and release of finished products
Perform supplier and vendor audits, as well as, Mock recall and internal audits
Any additional duties of assignments as directed by the Supervisor
Requirements
Minimum of Diploma or Bachelor degree (Life Sciences, Engineering, related profession).
Five+ years industry or related experience in cosmetic, device, food, or pharma
Previous inspecting, auditing or manufacturing experience – a plus
Data analysis, specification development skills
Computer literate and effective communication skills
Benefits
Medical, Dental, and Vision Insurance
Life Insurance
401k match
