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About the role

Director, Quality Assurance
Location: Greater Greenville, SC AreaSome relocation support offered
Lead enterprise-wide quality operations for my client in a highly regulated cGMP manufacturing environment. This is a high-impact leadership role driving compliance, continuous improvement, and product quality while building a culture of excellence. Why You Should ApplyLead Quality Assurance, QC Inspection, and Document Control Influence company-wide quality strategy and compliance Drive modernization of electronic Quality Management Systems Build and mentor a high-performing quality team
What You'll Be Doing:
  • Lead QA/QC operations, document control, CAPA, deviations, audits, and change control
  • Oversee material and finished goods release and batch certification
  • Ensure compliance with cGMP, FDA, OSHA, and regulatory requirements
  • Direct internal/external audits, supplier quality, investigations, and training
  • Champion continuous improvement and cross-functional quality initiatives
About You:
  • Bachelor's degree in a related field
  • Experience leading QA within a cGMP manufacturing environment
  • Strong knowledge of CAPA, change control, document control, audits, and quality systems
  • Proven leadership, coaching, and talent development skills
  • Excellent problem-solving, regulatory, and cross-functional communication abilities
How To Apply: We'd love to see your resume, but we don't need it to have a conversation. Send us an email to max@scientificsearch.com and tell me why you're interested. Or, feel free to email your resume. Please include Job#20006.#LI-MP1Type: Contract
Category: Pharmaceutical Manufacturing
Date Posted: 2026-09-11

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JOB OVERVIEW

Experience level

Manager

Location

Greenville, SC

Occupation

Quality Control Systems Managers

Industry

Pharmaceutical Preparation Manufacturing

Posted

41 days ago

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