Job Description


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Quality Engineer

  • Ref: 287660
  • Type: Direct Hire
  • Location: Ridgefield, NJ
  • Industry: Cosmetics / Skin Care
  • Job Level: Manager
  • Pay: Negotiable

Opportunity Description

A Global Cosmetics Company in the Ridgefield, NJ area is currently seeking a Quality Engineer for their facility.

Job Duties

  • Responsible for documentation of non-conformances, customer complaints, CAPA reports into QCBD, and lead investigations to close the documents to completion. 
  • Forward documents to the customer as necessary and respond to customer concerns with regards to quality. 
  • Develop and maintain documents which support the Quality Management System (QMS)
  • Responsible for project management/oversight of plant improvements. 
  • Interface with customers and review data during first production fill trials. 
  • Perform cGMP audits throughout the facility. 
  • Participate in the training of Line Leaders/Techs and Assembly personnel for new product fills. 
  • Support the internal quality auditing system.
  • Record and analyze data from first production fills and trial runs and communicate formal report and findings back to the production team and the customer. 
  • Play a key role in all customer and regulatory audits 
  • Develop and applies technical quality assurance protocols/methods for both product and process improvement. 
  • Ensures activities and items are in compliance with both company quality assurance standards and applicable government regulations
  • Performs analysis and identifies trends in products and processes and recommends corrective actions when necessary 
  • Support manufacturing operations from a quality perspective and participates in strategic development activities when requested Track quality assurance metrics Act as Quality Manager backup 
  • Perform other duties as needed or assigned 


  • Bachelor’s Degree in an applied science or engineering field

Experience & Skills Required

  • 3 years prior experience in Quality Assurance for personal care, OTC, Drug or device products
  • Knowledge of ISO 9001 and process improvement tools / techniques and experience
  • Familiar with Validation techniques
  • Must be able to combine and analyze quality data
  • Manage, execute, and track various validation projects. (Facility, Equipment qualifications, Cleaning/sanitizing validation, Software, Process Validation, and Change control)
  • Able to participate in a team-oriented environment, willingness to assist and train others
  • Demonstrate safe behavior and support department/plant safety goals in a continuous improvement process