Primary Skills: Commissioning Protocols (Advanced), Qualification Protocols (Advanced), GMP Knowledge (Advanced), Equipment Commissioning (Advanced), Report Generation (Advanced),
Contract Type: W2 Contract
Duration: 12 Months with Extension
Location: Thousand Oaks CA (Li, Hybrid)
Pay Range: $55.00 - $65.00 Per Hour
#LP
Job Summary:This role involves leading and executing commissioning and qualification efforts for new or modified GMP-compliant equipment, utilities, and facilities. You will be responsible for creating, reviewing, and implementing crucial testing documentation to ensure operational readiness. Collaboration with project teams and subject matter experts will be essential to define testing strategies and report on progress to stakeholders.
Key Responsibilities:
- Develop and execute commissioning and qualification test plans.
- Generate and review technical protocols and summary reports.
- Collaborate with cross-functional teams on testing strategies.
- Document and resolve any protocol deviations or issues.
- Communicate project status and progress to stakeholders.
Must-Have Skills:
- Experience in pharmaceutical/biotech C&Q roles.
- Strong understanding of cGMP commissioning and qualification practices.
- Proficiency in working with digital C&Q systems.
Experience in the pharmaceutical or biotechnology industry is required for this position.
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