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Msat Intern

Posted on May 6, 2025

  • Tuas, Singapore
  • 0 - 0 USD (yearly)
  • Full Time

Msat Intern
Posted Job Advert

Today, Lonza is a global leader in life sciences operating across five 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.

Did you know that we are the 1st biologics contract manufacturer in Singapore? We offer you exposure to upcoming biotech and established pharmaceutical companies and to the manufacturing technology needed to produce mammalian treatments and cell therapies of tomorrow. Our global manufacturing network is recognized for its reliable, high-quality services, regulatory track record, global footprint, innovative technology platforms and extensive experience – we, in Singapore are proud to be part of this global network.

The MSAT department is the process owner of cell culture or purification manufacturing processes (at mammalian biopharma sector). MSAT scientists/ engineers apply process development and engineering principles and concepts to new manufacturing processes, and perform continuous monitoring and support to existing manufacturing processes. The team also actively works on streamlining processes and improving process robustness. The Data Science team within MSAT is
focused on establishing an understanding of the performance of the cell culture and purification processes through process monitoring, in process control trending, data analysis and statistical modeling.

Job Activities

  • Build up understanding of cell culture/ purification process via daily process monitoring, in process control trending and data analysis
  • Compile presentations for Monitoring Review Board meetings
  • Support process investigations for control charting, control plan drafting and GDM object validation
  • Assist in special requests for data collection, completion and/or verification
  • Assist in resolving data entry related analytic problems with users
  • Assist in 6 monthly GDM user access review
  • Follows all training and policy guidelines established for the facility as well as all cGMP requirements. Ensures employee training profile is up to date at all times by regular monitoring of training lists (e.g. SAP Learning Portal) and completing all training in a timely fashion.
  • Any other duties as assigned by your Supervisor/Manager

Requirements

  • Diploma/ Degree in relevant science discipline (Biotechnology, Pharmaceutical Science, Chemical Engineering, Chemistry, Biochemistry or Biology) is preferred
  • Effective verbal and written communication skills
  • Ability to provide attention to detail
  • Demonstrate critical thinking skills and systematic approach
  • Strong interpersonal skills and positive team player
  • Proactive and willing to learn

Learning Outcomes

  • Basic understanding of cGMP working environment
  • Exposure to cell culture/purification processes at manufacturing scale
  • Exposure to Data Science methodologies, data management systems and statistical analyses
  • Time-management and task-prioritization skills

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.


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