The Attach and Train training period lasts for 15 months. Structured on-the-job training (OJT) will be provided and conducted at the participating companies to facilitate the application of learning and to ensure that individuals acquire necessary competencies to perform at their job.
This is a fully site‑based role at Singapore Tuas. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
The role is under Quality Control team, it follows a rotating shift schedule (12 hours day shift).
What you’ll get:
An agile career and dynamic working culture.
An inclusive and ethical workplace.
Daily company bus from the MRT location near your home to and from the Tuas site.
What you’ll do:
To prioritize and perform the various testing/analysis in timely manner, in order to support the business requirements.
Analysis of final product, in-process, raw material or environmental samples according to Standard Operating Procedures and Test Methods.
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.
Any other duties as assigned by your Manager.
Uphold data integrity principle in accordance to Lonza policies.
Proactively evaluate, identify and improve data integrity process
Understanding and execution of spectroscopy, and other assigned methods which may include chromatography methods (HPLC), TOC, Protein concentration (A280 or SoloVPE), osmolality, appearance and other
What we’re looking for:
Degree in a relevant Science field or equivalent
Individual without prior working experience in the biopharmaceutical manufacturing industry may also apply
Understanding of the application of mammalian cell culture for the production of biopharmaceuticals
Understanding of cGMP regulations
Good problem solving and analytical skills
Good communication and teamwork skills
Willing to perform rotating 12-hour shift pattern
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 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.
Lonza Singapore, Singapore, SGP Office
Singapore, Singapore
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