Job Description


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Quality Control Manager

  • Ref: 282884
  • Type: Direct Hire
  • Location: Port Jervis, NY
  • Industry: Cosmetics / Skin Care
  • Job Level: Experienced Non-Manager
  • Pay: Negotiable

Opportunity Description

We are currently seeking a Quality Control Manager to fulfill an opening we have in the Cosmetics/Skin Care industry.

Company Information

Our client, a company specializing in the manufacturing of cosmetics and skin care products; is an exciting and growing company to be a part of.

Job Duties

  • Assure the goal of the Quality Mission Statement is upheld in all decision processes.
  • Assure the Facility is compliant with all required Current Good Manufacturing Procedures and is aware of the Regulatory requirements for Product release.
  • Maintain the Quality System and ensures it is routinely revised to meet best practice.
  • Continuously assess ways to improve Quality Operations.
  • Create a Quality presence across the Organization.
  • Interface with customers on a routine basis.
  • Direct compliance to cGMP Regulations relative the Food & Drug Administration Regulations, CFR21, Parts 210 & 211.
  • Requires interface with the companies Leadership Team and their reports: Supervisors, Team Leaders, Compounders, Mechanics, Assemblers.
  • Utilize a risk-based approach for identifying areas of improvement and continuously improving by developing and implementing action plans to close potential gaps.
  • Primary Contact Person for Regulatory Audits (Food & Drug Administration).
  • Analytical Laboratories: Raw Material, In Process, Bulk, Finished Goods Analyses.
  • Deionized Water Analyses. Raw Material Retention Program. Microbiology Laboratories: Raw Material, In Process, Bulk, Finished Goods Analyses.
  • Environmental Monitoring Programs. Deionized Water Analyses. Preservative Challenge Evaluations. Sanitizer Validation Studies.
  • Product Quality Laboratories: Bulk physical testing, and shading for Lipstick, Personal Care and Powder products.
  • Finish product evaluations.
  • Bulk Product Retention Program.
  • Quality Number Reporting: Monthly Defective units by Operational area.
  • Weekly reporting on Quarantines and Customer Returns.
  • Quality Systems: Pharmaceutical Product Release Requirements.
  • Procedures--alignment with Current Good Manufacturing Practices.
  • Customer Standard Practice Instructions (SPI) Process--Definition, critical review of manuals and dissemination of information.
  • Documentation Retention Program.
  • Quality cGMP auditing of the Facility at required intervals.
  • Product Exception Release Policy / Process.
  • Quality Auditing Authority: Quality audits and resolution of issues surrounding on-line Quality Inspections of Operational areas.
  • Finish Product Retention Program.
  • Customer Return Authorization Process Primary Contact for Customer Audits and concomitants follow-up / corrective action.
  • Responsible for Regulatory Awareness and rolling out Regulatory principles to Operations.

Experience & Skills Required

Quality control and Quality Assurance in Science.