Specialist 1, Sample Management, QC

3 days ago

Tuas, Singapore Lonza Full time $60,000 - $80,000 per year

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.

As a QC Analyst, you will be responsible for managing QC samples (receipt, retention, and shipment), coordinating on-site and off-site archival of QC documents, overseeing equipment maintenance activities, and supporting the revision of operational procedures. You will also liaise with other departments to ensure timely delivery of results, compliance with standards, and smooth execution of laboratory operations.

What you will get

  • An agile career and dynamic working culture
  • An inclusive and ethical workplace
  • Compensation programs that recognize high performance
  • Daily company bus from the MRT location near your home to and from the Tuas site
  • Fully paid medical insurance, with the option to enroll family members at partially subsidized premiums
  • Opportunities to drive continuous improvement in a high-impact environment

What you will do

  • Manage QC samples, including receipt, storage, retention, and discard of process and raw material samples.
  • Control and audit retain samples to ensure compliance with procedures.
  • Coordinate Sample Logistics documentation and QC assay sheet issuance.
  • Write, maintain, edit, and review Standard Operating Procedures (SOPs).
  • Maintain data and records in compliance with cGMP and internal quality standards.
  • Manage and coordinate on-site and off-site archival of QC documents.
  • Perform stability pull samples according to defined time points.
  • Contribute to operational efficiency and continuous improvement initiatives.
  • Perform other duties as assigned by Supervisor/Manager.

What we are looking for

  • Degree or Diploma in Chemistry, Life Sciences, or a related field.
  • Relevant experience in QC sample management, laboratory operations, or documentation coordination.
  • Strong knowledge of cGMP regulations and quality systems.
  • Good problem-solving and analytical skills.
  • Strong communication skills with the ability to collaborate across functions.
  • A proactive team player with attention to detail and commitment to quality.

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.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law

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