Singapore, Tuas Singapore
Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
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 the MRT location near your home to and from the Tuas site
Fully paid medical insurance, with the option to enroll family members at partially subsidized premiums
Opportunities to drive continuous improvement in a high-impact environment
What You Will Do
Lead and execute small-scale liquid non-GMP media manufacturing runs to support scale-up and tech transfer activities
Support set-up, operation, calibration, and verification of pilot lab equipment and ensure equipment readiness
Manage formulation, preparation, and aseptic filling of non-GMP media batches, ensuring accurate documentation per SOPs
Analyze experimental data, summarize results, and prepare technical reports, protocols, and lab documentation
Assign raw material part numbers, prepare SDS, create batch labels, and generate Certificates of Test (COT) for non-GMP runs
Generate Bill of Materials (BOM) and raw material specification sheets for GMP runs as applicable
Prepare and submit samples to QC and coordinate external testing when required
Lead troubleshooting and provide technical recommendations for process improvements in pilot and scale-up studies
Support continuous improvement initiatives and ensure good laboratory practices, including 5S and safe work environment standards
Provide scientific expertise during investigations, audits, and customer interactions
Mentor and guide junior team members in laboratory operations and data analysis
Perform other duties as assigned by Supervisor/Manager
What We Are Looking For
Degree or Diploma in Biology, Chemistry, Biotechnology, or related field
5–10 years of relevant experience in biopharmaceutical operations, cell culture techniques, or media formulation development
Strong knowledge of cell culture media, upstream processing, and antibody production & purification processes
Experience in scale-up, technology transfer, and working with GMP manufacturing environments
Understanding of cGMP regulations and regulatory expectations
Strong problem-solving and analytical skills
Excellent communication and cross-functional collaboration skills
A team player who can work independently and contribute in a fast‐paced, dynamic environment
Lonza is an equal‐opportunity employer.
All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
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