CCP Trainee, MSAT MM

Lonza is the pioneer and world leader in the CDMO industry operating across 5 continents, setting the pace with cutting‐edge science, smart technology and lean manufacturing. We turn our customers' break‐through innovations into viable therapies and manufacture the medicines of tomorrow. At the heart of every scientific breakthrough are talented individuals collaborating to develop solutions that empower businesses to improve lives. 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. Join our best‐in‐class high performance Integrated Biologics team at our Tuas site in Singapore to gain unparalleled exposure to cutting‐edge biotechnology and innovation, and make a difference from day one. Learn new skills and capabilities, and grow your career with us in manufacturing therapeutic proteins under cGMP conditions. Find out more about what a life at Lonza in Singapore could look like for you by watching this short video. The Career Conversion Program (CCP)training period lasts for 15 months. Structured on‐job training (OJT) will be provided and conducted at the participating companies to facilitate the application of learning and to ensure that individuals acquire necessary competencies to perform at their job. Team Overview The MSAT (Manufacturing Science and Technology) USP (Upstream Processing) team at Lonza Singapore is responsible for the technical oversight of upstream processes at Lonza Singapore mammalian biopharmaceutical drug substance manufacturing facility. The team plays a key role in implementing process changes, monitoring process performance during clinical and commercial manufacturing campaigns, and supporting product commercialization activities such as finalizing the commercial process design, preparing Process Performance Qualification (PPQ) and regulatory submissions. What you'll do As a trainee in the MSAT USP Process team, you will be involved in: Pre‐campaign preparation activities , including change implementation via change requests and revisions of GMP documentation. Process monitoring during manufacturing campaigns , such as compiling and reviewing process data, investigating issues, troubleshooting through data mining and analysis, and providing performance updates to relevant stakeholders. Post‐campaign performance reviews and planning for subsequent manufacturing campaigns. Supporting product commercialization efforts , including conducting Process Failure Mode and Effects Analysis (FMEA), analyzing Process Characterization data, and defining commercial process ranges for PPQ and the overall Process Control strategy. Collaborating closely with cross‐functional teams , including Manufacturing (MFG), Quality Assurance (QA), Quality Control (QC), and Process Development. What we are looking for A strong desire to learn and apply new knowledge. Great interpersonal, oral, and written communication skills. Critical thinking and resourcefulness in problem‐solving. High attention to detail. A collaborative and proactive team player. 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. #J-18808-Ljbffr