Analyst, QC (Environmental Monitoring)

Lonza Group Ltd.; Singapore; Presencial; SGD 52 000 - 76 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Medical insurance

Transport to site

Shift allowances

Career growth

Resumo da oferta

The Lonza Group Ltd. in Singapore is seeking an Analyst QC, Environmental Monitoring (EM) to perform environmental monitoring in cleanrooms and manufacturing areas, ensuring GMP quality and safety standards for life‑saving medicines.

This fully site-based shift role offers hands-on collaboration, real‑time problem solving, and opportunities to contribute to cGMP compliance, data integrity, and continuous improvement within a global life sciences leader.

Qualificações

• Degree in science or related field.
• Relevant work experience in Pharmaceutical Manufacturing or Biopharmaceutical industry.
• Knowledge of regulatory requirements (FDA, EMEA, ICH Q7).
• Team player with strong focus on safety, quality and timelines.

Responsabilidades

• Perform microbiological testing (bioburden, LAL, plating/counting, microbial identification, EM sampling).
• Conduct environmental monitoring (air, surface, viable, non‑viable) across manufacturing/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, inventory).
• Manage sample logistics including retention samples, external testing coordination, 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.

Conhecimentos

Bioburden testing

LAL testing

EM sampling

GMP compliance

Formação académica

Degree in science

Descrição da oferta de emprego

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.

Ready to shape the future of life sciences?

Every day, our teams across the world work together to turn scientific breakthroughs into life-changing medicines that reach up to 100 million patients a year. Lonza is a place where people can make a unique impact, grow their careers and belong.

You will feel at home at Lonza if you:

• Take ownership, step forward, and enjoy meaningful responsibility
• Love solving problems and thrive in a complex, fast‑moving environment
• Are curious, always looking to learn and improve
• Work collaboratively, contributing to something bigger than yourself
• Are motivated to make a difference through work that impacts customers and their patients

Why Lonza: We are a place of unique opportunity, where your ideas, expertise and ambition can make a real difference. Here, you will have the freedom to grow, the support to succeed and the chance to contribute to work that matters. We are the makers of the medicines of tomorrow. Join us. Be you.