Our client is a leading biopharmaceutical company dedicated to developing innovative therapies to improve patient outcomes. Their mission is to advance science and transform lives through cutting-edge research and development.
Role: QC Technical Expert
Responsibilities:
- Supervise testing techniques and scheduling
- Review laboratory data and close out deviations
- Author and review Change Controls, Deviations, Test Methods, Specifications, and SOPs
- Solve analytical/microbiological method issues and troubleshoot equipment
- Manage equipment qualification and validation
- Lead method transfers and validation
- Participate in quality improvement initiatives (e.g., Lean Six Sigma)
- Analyze quality metrics data
- Conduct Risk Assessments
- Make decisions in areas of expertise
- Support audits
- Perform other duties as assigned
Qualifications:
- Bachelor's or Diploma in a relevant science field
- Minimum 10 years of Quality experience in a GMP environment
- Strong understanding of QC activities and lab functions in biotechnology or medical devices
