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.
Key Responsibilities:
- Point of contact in the department for laboratory support and inventory matters
- Performs laboratory support services assisting the dept in running an efficient laboratory. Includes but not limited to housekeeping, preparing buffers, media, routine calibration of equipment and maintaining inventory levels by working closely with delivery and stores personnel.
- Has an area of expertise in the lab and a good understanding of a subset of equipment. Able to apply expertise and perform standard laboratory activities such morning verifications, equipment data and time check etc
- Drives and implements improvement activities using laboratory expertise and OE concepts
- Equipment owner and trainer for equipment or lab activities
- Liaise with other Lonza departments and vendors for inventory and equipment matters
- Point of contact in the department for equipment calibration, preventive maintenances, etc
- Perform equipment validation and qualification, equipment requalification, equipment maintenance and troubleshooting etc
- Perform Equipment Validation Maintenance Quality Systems review and re-qualification activities to ensure GMP equipment is continuously maintained in a validated state
- Perform change control assessments for GMP equipment and associated validation activities to ensure compliance with regulatory requirements
- Perform assigned Quality Systems activities including: Document Management System (DMS), and Track Wise system (Change Control, Deviations, CAPA, etc)
- Any other duties as assigned by Management
Key Requirements:
Experience and understanding of laboratory equipment and associated quality systems
Understanding of cGMP regulations
Strong technical writing skills and ability to document all work in a meticulous, accurate, and timely manner
Strong written, oral communication skills and ability to work interdepartmentally with very minimal supervision in an effective manner to carry out daily duties
Understand how to write discrepancies, give a root cause analysis and perform Quality Risk Assessments
Strong organizational and time management skills
Excellent communication skills
Excellent teamworking skills
Demonstrates ability to prioritize tasks as needed to support the changing business demands
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 achieved 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.
