Analyst, QC (Environmental Monitoring)

Lonza; Singapore; On-site; Confidential; Full time

Benefits offered by this job

Medical insurance

Shift allowances

Transport provided from MRT to Tuas

Career growth opportunities

Global exposure

Job summary

Lonza in Singapore is seeking an Analyst QC, Environmental Monitoring to perform microbiological testing and EM sampling across manufacturing and cleanroom areas. You will ensure GMP compliance and data integrity while supporting investigations and trending.

The role operates on a fully site-based shift, requiring in-person collaboration to maintain the highest quality and safety standards in medicine manufacturing.

Qualifications

• Degree in science or related field required.
• Experience in Pharmaceutical Manufacturing or Biopharmaceutical industries preferred.
• Familiar with regulatory requirements and local codes & standards (FDA/EMEA/ICH Q7).
• Knowledge of GMP quality management systems and data integrity.

Responsibilities

• Perform microbiological testing (bioburden, LAL, plating/counting, microbial ID).
• Conduct environmental monitoring (air, surface, viable, non-viable) in manufacturing and cleanrooms.
• Analyze raw materials, in-process, environmental, and final product samples per SOPs and GMP.
• Document, review, and report results in compliance with cGMP and data integrity standards.
• Support trending, investigations, and deviation/OOS activities with root-cause analysis.
• Maintain lab operations: equipment upkeep, housekeeping, reagents, and inventory control.
• Manage sample logistics and external testing coordination.
• Prepare and maintain GMP-compliant standards and reagents.
• Ensure timely testing and reporting to meet production needs.
• Participate in peer reviews and continuous improvement initiatives.

Skills

Team player

Independent worker

Safety-focused

Quality focus

Timelines

Education

Degree in science or related field

Job description

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.

What we’re looking for

• 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.