About this role
As an Analyst QC, Environmental Monitoring (EM) you will perform environmental monitoring activities to ensure cleanroom and manufacturing areas consistently meet GMP quality and safety standards essential for the production of life-saving medicines.
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 site‑based shift role. Working together in person supports close, real‑time 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.
Shift allowances.
Access to Lonza’s full suite of employee benefits: www.lonza.com/careers/benefits
What you’ll do
Perform microbiological testing (bioburden, LAL, plating/counting, microbial identification, EM sampling, particulate monitoring).
Conduct environmental monitoring (air, surface, viable, and non-viable sampling) across manufacturing and cleanroom areas.
Analyze raw materials, in-process, environmental, and final product samples per SOPs and GMP requirements.
Document, review, and report results in compliance with cGMP and data integrity standards.
Support trending, investigation, and deviation/OOS activities, including root cause analysis.
Maintain laboratory operations (equipment upkeep, housekeeping, reagents, consumables, and inventory control).
Manage sample logistics including retention samples, external testing coordination, and QC documentation/shipping.
Prepare and maintain GMP-compliant standards and reagents.
Ensure timely testing and reporting to meet operational and production needs.
Participate in peer review and continuous improvement initiatives.
Uphold strict data integrity and GMP compliance at all times.
Perform additional duties as assigned by the manager.
Degree in science or related field
Relevant work experience in Pharmaceutical Manufacturing industry or Biopharmaceutical industry
Familiar with Regulatory requirements and local Codes & Standards (e.g., FDA, EMEA, and ICHQ7)
Knowledge and experience of the practical and theoretical requirement of quality management system in GMP facility
Team player who can operate independently, with strong focus on safety, quality and timelines
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.
About Lonza
Swiss contract development and manufacturing organization (CDMO) providing biologics, cell, and gene therapy production services.
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