Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Did you know that we are the 1st biologics contract manufacturer in Singapore? We offer you exposure to upcoming biotech and established pharmaceutical companies and to the manufacturing technology needed to produce mammalian treatments and cell therapies of tomorrow. Our global manufacturing network is recognized for its reliable, high-quality services, regulatory track record, global footprint, innovative technology platforms and extensive experience – we, in Singapore are proud to be part of this global network.
The role will support the quality operations department in Cell Therapy and is responsible for planning & supporting Cell Therapy operations. The aim of this position is to develop fill-finish expertise to support the flawless execution of the Cell & Gene Therapy production process.
Key responsibilities:
- Support day-to-day Quality Assurance activities in accordance with approved SOPs / Policies for a large scale, multi-product, GMP biotech manufacturing facility.
- Planning for future activities and coordinate with other departments on projects and issues
- Develop in depth awareness of entire process; identifying operational factors which influence the process.
- Participate actively or lead in deviation investigations, change controls, CAPA plans, supplier change notifications, complaints, and closure of discrepancy reports.
- Ensure real-time decisions on process events on the floor based on knowledge of defined SOPs & policies.
- Develops good working relationships with internal & external customers.
- Participate in internal audit / regulatory inspections / customer audits
- A competent Reviewer and Approver of SOPs, protocols, reports or records.
- Identify process pathways and work to develop improvements in strategy.
- Any other tasks as and when assigned by supervisor.
Key requirements:
- Bachelor's degree with experience in Quality Assurance in the Biopharmaceutical industry.
- Relevant QA Operations background with experience supporting manufacturing operations.
- Experience in deviation investigation, change control and CAPA activities.
- Hands-on experience coordinating & interacting with internal departments on manufacturing activities.
- Fair knowledge and experience of the practical and theoretical requirement of quality management system in a GMP facility.
- Meticulous and Systematic.
- Team player, with strong focus on safety, quality and timelines.
Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieve ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
