Analyst, QC (12 months contract)
Singapore, Tuas Singapore
Today, Lonza is a global leader in life sciences operating across five 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.

Duties and Responsibilities:

  • 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

Education / Experience

  • Degree/Diploma in a relevant Science field or Equivalent
  • 5-10 years of QC experience, preferably in biotech, healthcare, or life sciences.
  • Expertise in bioassays (ELISA, PCR, FACS) and ability to maintain quality standards while achieving results.
  • Strong analytical and decision-making skills, with a desire to continuously learn and grow.
  • Experience with USP 71 Sterility testing is preferred

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.

Reference: R63795