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Quality Control (FG) Manager - Cosmetics & Skincare

Englewood Lab, Inc.
locationPaterson, NJ, USA
PublishedPublished: 6/14/2022
Manufacturing
Full Time

Job Description

Job DescriptionTitle: Quality Control FG Manager
Reports to: Head of Quality
Department: Quality Control

Responsibilities:

  • Scheduling of QC Inspectors for Incoming Components Receiving; Raw Material Receiving Inspection, Manufacturing/Production areas, Warehouse FG auditing, Special Sample handling, Review of Inspection Records, including but not limited to: In-coming Inspection records; In-process Batch Records and related documentation.
  • Conduct non conformance, product complaints, out-of-specification investigation and provide corrective and preventive actions with follow-ups as related to QC activities.
  • Trains and supervises document review personnel; Incoming Inspection records, batch release personnel, issues certificates of conformance (COC), certificates of manufacture (COM), and certificates of analysis (COA) to customers on bulk and work-in-progress (WIP). Maintains accurate record of approved, quarantined, rejected products.
  • Ensure compliance to all SOPs and other regulatory requirements (e.g. FDA, EPA, OSHA, ISO 13485:2003).
  • Maintain working knowledge of OTC Drug requirements for incoming materials and ingredients; components (primary and secondary); intermediates, bulk and FGs.
  • Reviews, Approve, Release, Quarantine or Reject per compliance inspection and testing such materials as: Incoming OTC and Cosmetic RMs; Incoming bulk and intermediates; Incoming Components; where applicable, to customer requirements.
  • 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/Production and Warehouse 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 for pre-weigh and bulk manufacture and makes recommendations.
  • Assist in interpreting and/or developing of customer specifications and requirements for approved formulas.
  • 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 & Pdn/Assembly in-process Specifications (F/As).
  • Reviews of batch records, fill cards, 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.
  • 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, when applicable.
  • Perform supplier and vendor audits, as well as, Mock recall and internal audits.
  • Ensure compliance to Product Quality Review stipulations.
  • Perform the functions of Authorized Person (AP) for goods and materials.
  • Maintain working knowledge of QC Analytical testing including IR, pH, Refractive Index, Viscometer, Spectrophotometry, Vacuum tester, and other Instrumentation.
  • Maintain working knowledge of MIL-STD/ANSI/ASQ Sampling and Testing.
  • Maintain Standards, Range boards, and Retain Samples Program

Qualifications:

  • Minimum of 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.
  • Ability to lift and carry up to 10-15 pounds.

Compensation & Benefits:

  • Medical, Dental, and Vision Insurance
  • Life Insurance
  • 401k match
  • PTO

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