Analyst, QC (Microbiology-Shift)

As a QC-Analyst (Microbiology-Shift) you will support routine QC sampling and testing for environmental and product samples (Eg. bioburden testing, endotoxin testing, etc). This role will be required to perform shift. 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. Access to Lonza’s full suite of employee benefits: What you’ll do: Perform microbiology and environmental monitoring (EM) testing on raw materials, in-process samples, bulk products, and environmental samples. Conduct microbiological tests such as bioburden, LAL, microbial plating and counting, and microbial identification. Review and document test results accurately in compliance with cGMP, SOPs, and approved test methods. Monitor and analyze microbiological trends, identify unusual results, and prepare required reports. Support laboratory investigations and troubleshooting when there are unexpected or out-of-specification results. Troubleshoot analytical methods and laboratory equipment and help resolve technical issues. Participate in method transfer, method validation, equipment qualification, and selection of QC equipment, standards, and reagents. Support process and environmental microbiology investigations when required. Maintain the laboratory, including equipment maintenance, housekeeping, and inventory management of laboratory supplies. Ensure all laboratory activities and documentation are completed accurately and in accordance with cGMP requirements. What we’re looking for: Degree/Diploma in a relevant Chemistry, Science field or Equivalent. Relevant experience and accomplishment to dictate final position for which the candidate may qualify. Well versed in cGMP regulations. Knowledge of area specific responsibilities. Good problem solving and analytical skills. 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? Apply now.