Specialist 1, Sample Management, QC

Specialist 1, Sample Management, QC

Apply locations SG - Tuas, Singapore time type Full time posted on Posted 2 Days Ago job requisition id R64849

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.

This role is responsible to coordinate and manage QC samples (receive, retain, shipment), manage and coordinate on-site/off-site archival of QC documents, coordinate equipment maintenance and revision of related operation procedure. Role is also required to coordinate with the other departments to ensure timely delivery of samples/results and equipment maintenance performed.

Key responsibilities:

1. To manage QC samples (including receipt, storage and discard of samples).
2. Control and audit of retain samples (process and raw materials).
3. Coordination of Sample Logistics documentation and QC assay sheet issuance.
4. Write, maintain, edit and review Standard Operating Procedures.
5. Maintain data and records in compliance with regulatory requirements and Standard Operating Procedures.
6. Manage and coordinate on-site/off-site archival of QC documents.
7. Perform stability pull samples according to stipulated time points.
8. Actively contributes to operational efficiency/continuous improvement initiatives.
9. Any other duties as assigned by your Supervisor/Manager.

Key Requirements:

1. Degree/Diploma in a relevant Chemistry, Science field or Equivalent.
2. Relevant experience and accomplishment to dictate final position for which the candidate may qualify.
3. Well versed in cGMP regulations.
4. Knowledge of area specific responsibilities.
5. Good problem solving and analytical skills.
6. Good communication skills.
7. A key team player.

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.