Biotechnologist, MCO (Mammalian)

Lonza Group

Singapore

On-site

SGD 50,000 - 80,000

Full time

4 days ago
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Benefits offered by this job

Daily bus to Tuas site
Fully paid medical insurance
Shift allowances & development
Inclusive workplace
Global benefits info on Lonza site

Job summary

Lonza is seeking a Biotechnologist to join the MCO-MEP team at our Tuas site in Singapore. You will support drug substance manufacturing by preparing materials, equipment and cleanrooms in a cGMP environment, gaining hands-on experience with biopharma processes.

Role requires technical aptitude, ability to operate DeltaV and work in shifts. You will collaborate with cross-functional teams to ensure safe and compliant operations while maintaining documentation and quality standards.

Qualifications

  • NITEC, Diploma or Degree in Biotechnology, Biochemistry, Chemical/Biochemical Engineering, Life Sciences or related discipline.
  • Basic understanding of cGMP requirements and data integrity principles.
  • Strong technical aptitude with willingness to learn equipment operations and basic process troubleshooting.

Responsibilities

  • Perform material and equipment preparation activities in a cGMP manufacturing environment per approved procedures.
  • Prepare, monitor and maintain manufacturing equipment and cleanroom areas, including sanitation and 6S housekeeping.
  • Conduct basic lab tasks including sampling, pH, conductivity and osmolality measurements with aseptic techniques.
  • Execute manufacturing activities using SOPs and Batch Records; support sample submission via LIMS with compliant documentation.
  • Develop competency in manufacturing equipment, process parameters and DeltaV operations.
  • Support quality/compliance activities including deviations, environmental monitoring, doc revisions and data integrity.
  • Collaborate with Manufacturing, MSAT, QA and cross-functional teams to troubleshoot issues and maintain schedules.

Skills

Technical aptitude
Team player
Communication skills
Cleanroom hands-on
Documentation
12-hour shifts

Education

NITEC/ Diploma/ Degree in Biotechnology or related field

Tools

DeltaV
LIMS

Job description

We have a great opportunity for a Biotechnologist to join our Manufacturing Central Operations - Material & Equipment Preparation (MCO-MEP) team at our Tuas site in Singapore. As a Biotechnologist, you will support the manufacture of therapeutic proteins by ensuring materials, equipment and manufacturing areas are prepared and ready for cGMP operations. Working in a cleanroom environment, you will gain hands-on experience with biopharmaceutical manufacturing processes and equipment while contributing to safe, compliant and efficient 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 MRT locations across Singapore to and from our Tuas site.
  • Fully paid medical insurance, with the option to enroll family members at partially subsidized premiums.
  • Shift allowances and ongoing learning and professional development opportunities.
  • Our full list of global benefits can be found on the Lonza Careers - Benefits page.
What you will do
  • Perform material and equipment preparation activities in a cGMP manufacturing environment, following approved procedures and safety requirements.
  • Prepare, monitor and maintain manufacturing equipment and cleanroom areas, including routine sanitization, 6S housekeeping, suite stocking and Kanban activities.
  • Perform basic laboratory and operational tasks including sampling, pH, conductivity and osmolality measurements, while applying appropriate aseptic techniques.
  • Execute manufacturing activities using SOPs, Batch Records and logbooks, and support sample submission through LIMS while maintaining accurate and compliant documentation.
  • Develop competency in manufacturing equipment, critical process parameters and operational workflows, including DeltaV operations and standard batch/changeover progression.
  • Support quality and compliance activities including deviations, environmental monitoring events, document revisions, validation activities and data integrity requirements.
  • Collaborate with Manufacturing, MSAT, QA and other cross-functional teams to troubleshoot operational issues, maintain production schedules and drive safe and efficient operations.
What we are looking for
  • NITEC, Diploma or Degree in Biotechnology, Biochemistry, Chemical/Biochemical Engineering, Life Sciences, Engineering or a related discipline.
  • Relevant experience in pharmaceutical, biopharmaceutical, manufacturing or cleanroom operations is preferred; candidates with relevant technical training are also encouraged to apply.
  • Basic understanding of cGMP requirements, manufacturing procedures and data integrity principles is an advantage.
  • Strong technical aptitude with the willingness to learn equipment operations, material preparation and basic process troubleshooting.
  • Positive and proactive team player with strong communication and interpersonal skills and the ability to adapt to changing operational priorities.
  • Ability to perform hands-on work in a cleanroom environment, including prolonged standing, equipment movement and manual handling of items up to 12 kg.
  • Willingness to work a rotating 12-hour shift pattern and maintain the required training and operational competencies.
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.

  • 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, 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.

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