Quality Assurance Supervisor - Cosmetics & Skincare

• Support Investigations (e.g. non conformance, product complaints, out-of-specification investigation and provide corrective and preventive actions with follow-ups).
  
• Train and supervise document control/review personnel; batch release personnel, accurate record of approved, quarantined, rejected products.
  
• Lead the review, release and compliance of materials, FG, bulk and intermediates where applicable, to support customer requirements.
  
• Support audits, inspections and ensure compliance to all SOPs and other regulatory requirements (e.g. FDA, HC, EPA, OSHA, ISO 13485:2016).
  
• Familiar with US FDA OTC drug regulations, including data integrity requirements.
  
• Maintains a working knowledge of QA inspection requirements for components, raw materials, in-process/bulk and finished goods.
  
• Ensures that review of in-process activities in both Manufacturing and Warehouse areas is conducted by QA 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 & Assembly in-process Specifications.
  
• Reviews of batch records, work sheets, and Inspection documentation for completeness and correctness.
  
• Support non-conformance resolutions, complaint investigations, and associated corrective and preventative actions.
  
• Reviews of QA 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 bulk and finished products, when applicable.
  
• Perform supplier and vendor audits, as well as, Mock recall and internal audits.
  
• Support Process Validation and Cleaning & Sanitization Validation activities under the quality systems to ensure compliance.
  
• Support formal drug stability program, bulk hold studies, and product compatibility by co-ordinating samples submission, testing, result retrieval and program review.
  
• Maintains files and database of customer-approvals and documents as evidence of authenticity.
  
• Effects changes to specification sheets as approved through proper change control requests.
  
• Support Change Control Requests for Customer requested changes to raw material, intermediate/bulk, FGs, specifications.
  
• Maintains copies of approved change controls as applicable to product specification updates/revisions.
  
• Under the supervision of Quality Manager, review and approved formulas, specifications and procedures.
  

Communicates new and updated SOPs to all employees at EWL.

• Three + years industry or related experience in cosmetic, device, food, or pharma.
  
• Experience/Knowledge of US FDA OTC regulations - a plus.
  
• 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.
  

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

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