Section Lead, QC (CGT)

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.

As a Senior QC Analyst, you will leverage your technical expertise in a variety of testing techniques and collaborate with cross-functional teams to ensure timely project delivery.

Responsibilities:

1. Provide technical leadership in biochemical testing, including cell counts, flow cytometry, ELISA, PCR analysis, and compendial testing (pH, Conductivity, Appearance) as per USP, JP, and EP standards.
2. Troubleshoot equipment and method-related issues by analyzing data and trends to resolve problems.
3. Collaborate with tech transfer teams to introduce new processes or modify existing ones, acting as the lab's designated point of contact.
4. Lead complex projects, coordinating various project teams to ensure successful completion and effective communication across all stakeholders.
5. Prepare and manage project documentation, including Method Transfer, Qualification, Validation reports, and product stability programs.
6. Oversee preventative maintenance and requalification of stability-related equipment.
7. Contribute to Annual Product Reviews and regulatory documents and provide guidance to junior staff.
8. Support continuous improvement initiatives and participate in audit activities when needed.
9. Proactively communicate risks to managers and the Head of QC.

Requirements:

1. Degree in a relevant scientific field or equivalent.
2. 5-10 years of QC experience, preferably in biotech, healthcare, or life sciences.
3. Expertise in bioassays (ELISA, PCR, FACS) and ability to maintain quality standards while achieving results.
4. Strong analytical and decision-making skills, with a desire to continuously learn and grow.

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.