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Lonza

Associate Specialist / Specialist, Lab Services, DS

Reposted One Month Ago
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In-Office
Singapore, SGP
Entry level
In-Office
Singapore, SGP
Entry level
Support day-to-day GMP laboratory operations including buffer/media prep, equipment checks, environmental monitoring, documentation, coordination with teams, and continuous improvement initiatives while maintaining data integrity and EHS compliance.
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Find out more about what a life at Lonza in Singapore could look like for you by watching this short video.

This is a fully sitebased role. Working together in person supports close, realtime collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

What you’ll get

  • An agile career and dynamic working culture in a global life sciences leader.

  • An inclusive and ethical workplace that values diversity and integrity.

  • Competitive compensation programs that recognize high performance.

  • Professional growth opportunities through cross-functional projects and global exposure.

  • Comprehensive medical insurance, with the option to enroll family members at partially subsidized premiums.

  • Company transport provided from designated MRT locations to and from the Tuas site.

  • Access to Lonza’s full suite of employee benefits: www.lonza.com/careers/benefits

What you’ll do

  • Comply with EHS regulations and cGMP requirements at all times.

  • Accurately document activities and results in accordance with Lonza policies.

  • Support daily laboratory operations, including housekeeping, buffer/media preparation, equipment checks, and environmental monitoring.

  • Coordinate with internal departments, vendors, and logistics teams.

  • Contribute to continuous improvement initiatives using Operational Excellence (OE) tools.

  • Maintain and promote data integrity in line with company policies.

  • Perform other duties as assigned by management.

What we’re looking for

  • Diploma or Degree in a relevant Science discipline or equivalent.

  • Experience with laboratory equipment, validation, maintenance, and quality systems.

  • Good understanding of cGMP regulations and GMP documentation practices.

  • Ability to perform root cause analysis, quality risk assessments, and technical documentation.

  • Strong organizational, communication, and teamwork skills.

  • Able to prioritize tasks, work independently, and adapt to changing business needs.

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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