Associate Director, QA (R&D)

Tarsus PharmaceuticalsIrvine, CA
5h$150,000 - $210,000Hybrid

About The Position

Reporting to the Director, Quality Assurance, the Associate Director, R&D Quality Assurance is responsible for managing early-stage contract drug product manufacturers, contract packagers, contract testing labs, contract raw material manufacturers and contract warehouses from a supplier quality perspective. This position is responsible for review and approval of investigations for production deviations and laboratory OOS; review and approval of change controls for master manufacturing records and test methods; test method validation protocols and reports; drug product, API and label specifications; review of master and executed batch records; and product disposition. This position also supports vendor management, supplier audits and quality agreements. Let’s talk about some of the key responsibilities of the role:

Requirements

  • Bachelor’s Degree plus 12+ years experience in the Pharmaceutical Industry
  • 7+ years experience in Pharmaceutical Quality Assurance
  • Experience with investigations using root cause analysis, CAPA and CAPA effectiveness
  • Strong attention to detail
  • Proficient technical skills across multiple platforms
  • Strong knowledge of Microsoft Office Systems
  • Analytical skills to interpret statistical data Preferred

Responsibilities

  • Attend Project Team Meetings; collaboration with Pharmaceutical Sciences and Program Management
  • Participate in vendor calls
  • Review and approve Vendor Change Controls
  • Review and approve vendor documents including Master Manufacturing Records and Master Packaging/Labeling Records
  • Review and approve all specifications
  • Review/Approve Deviations/OOS
  • Review/Approve Test Record Form/Certificate of Analysis
  • Review executed manufacturing batch records and packaging/labeling batch records
  • Review/Complete Batch Record Review Form
  • Complete Final Disposition Form and issue Certificate of Compliance
  • Author/Revise Quality Assurance Procedures
  • Review and Approve Pharmaceutical Sciences SOPs
  • Perform audit report review of audits performed by 3rd party auditors
  • Attend Supplier Audits, as needed
  • Review proposed Quality Agreements

Benefits

  • health, dental and vision insurance benefits
  • generous paid time off, including vacation, holidays, and personal days
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