Biotechnician I

Responsibilities

• Execute drug product formulation, filling, lyophilization, visual inspection, labeling, and packaging
• Perform cGMP manufacturing operations including equipment cleaning, sterilization, and solution preparation
• Conduct sterile filtration, integrity testing, and environmental monitoring
• Manage equipment start-up, troubleshooting, and acceptance testing
• Maintain strict adherence to Good Documentation Practices (GDP) and SOPs
• Operate within ISO5, ISO7, and ISO8 cleanroom environments using aseptic gowning techniques

Requirements

• Demonstrated ability to successfully gown into aseptic manufacturing areas
• Experience with cGMP manufacturing and Good Documentation Practices
• Proficiency in sterile filtration and environmental monitoring
• Strong organizational and time-management skills to handle heavy workloads and aggressive timelines
• Proficiency with Microsoft Office (Excel, Outlook, Word)
• Ability to stand for long periods (8-12 hours) and lift up to 40 lbs
• Flexibility to work 1st or 2nd shift, including holidays, weekends, and overtime as needed

About the Company

BeiGene is a global oncology company dedicated to discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a global team of over 11,000 colleagues, we are committed to radically improving access to medicines through bold ingenuity and a collaborative spirit.