- An agile career and dynamic working culture in a global life sciences leader.
- An inclusive and ethical workplace that values diversity and integrity.
- Competitive compensation programs that recognize high performance.
- Professional growth opportunities through cross-functional projects and global exposure.
- Comprehensive medical insurance, with the option to enroll family members at partially subsidized premiums.
- Company transport provided from designated MRT locations to and from the Tuas site.
- Access to Lonza's full suite of employee benefits:
- Understanding and execution of Biochemical such as cell counts, flow cytometry, ELISA, PCR analysis, and compendial testing (pH, Conductivity, Appearance) as per USP, JP, and EP standards.
- Documentation and review of results in accordance with current Good Manufacturing Practices (cGMP).
- General lab support including housekeeping, equipment maintenance, inventory of supplies, lab supplies ordering, management of glass wares, autoclaving etc.
- Support sample logistics area including retention sample storage, external lab test, QC documents control, shipment of QC samples. Prepare, maintain standards and reagents as required by GMP documents. Responsible to follow data integrity requirements.
- Actively contributes to operational efficiency/continuous improvement initiatives. Problem solving of analytical methods as well as troubleshooting of
- equipment. Involved in equipment qualification, maintenance and troubleshooting. Support / Perform OOS, deviation investigations. Draft investigations reports.
- Any other duties as assigned by your Supervisor/Manager
- Degree/Diploma in a relevant Science field or Equivalent
- 0-5 years' experience in Quality Control
- Strong knowledge of microbiological laboratory operations in a manufacturing environment
- Demonstrates an ability and desire to learn from experience
- Good problem solving and analytical skills
- Good communication skills
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Analyst 2, QC - Tuas - Lonza
Description
Singapore, Tuas SingaporeAs a QC-Analyst the role is responsible for executing and supporting a broad range of biochemical testing activities in compliance with GMP standards. The position ensures data integrity, operational excellence, and regulatory compliance through accurate documentation, equipment management, investigation support, and continuous improvement initiatives within the QC laboratory.
What You'll Get
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 value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
Reference: R72939
Apply
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