Senior Production Support, Biotechnologist

What You’ll Do

• Material & Equipment Staging: Lead the technical coordination, staging, and movement of all process-critical materials, consumables, and equipment (including single-use bioreactor assemblies and hardware) to prevent floor delays.
• Weigh & Dispense: Support production of media and buffers by weighing components to be used in media/buffer formulation.
• Suite Readiness & On-Time Delivery: Support the development and execution of robust suite readiness checklists, ensuring manufacturing teams are fully set up for flawless campaign execution.
• Cross-Functional Procurement Tracking: Partner with internal supply chain and materials specialists to track purchase requisitions, manage BOM inventories, and monitor deliveries against strict project metrics.
• Technical Transfer Operational Support: Provide crucial operational and material-flow support during tech transfer milestones, including facility water runs, particle runs, and engineering runs.
• Documentation Compliance: Author, review, and execute GMP documentation—including Standard Operating Procedures (SOPs), Work Instructions (WIs), and material tracking sheets—ensuring total GDP compliance.
• Direct Manufacturing Assistance: Maintain processing proficiency across core unit operations (e.g., cell growth, harvest, or fill/finish) to seamlessly jump in and directly assist manufacturing teams on the floor as production demand dictates.
• Quality & EHS Alignment: Manage daily tasks in strict compliance with site safety objectives and cGMP guidelines, actively participating in room clearance, facility sanitization, and the resolution of material-related deviations.

What We’re Looking For

• Experience: 5+ years of experience within a cGMP biological manufacturing or regulated clinical laboratory environment is required.
• Technical Background: Background identical to a standard manufacturing associate, including an understanding of aseptic techniques, hygienic processing concepts, and basic microbiology principles.
• Skills: Excellent proactive communication, strong computer literacy, and superior organizational skills required to coordinate complex material requirements across multiple internal departments.
• Adaptability: Ability to think quickly, draw accurate conclusions, and thrive under the dynamic, shifting priorities of an active pharmaceutical manufacturing asset.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law.