Quality Control jobs in United States

Singapore, Tuas Singapore

Role is required to have an understanding and execution of Bioassay and Environmental Monitoring techniques with regards to the testing of environmental, in-process and final product samples. QC testing includes but is not limited to: Total particulates, Air viable, Surface viable, cell count, flow cytometry, sterility testing and ELISA. Role is also responsible for tracking and review of external tests which includes but not limited to: sterility, virus and mycoplasma testing for all products (as required).

• 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, and option to enrol family members at partially subsidized premiums.

Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits.

• To prioritize and perform the various testing/analysis in timely manner, in order to support the business requirements.
• Analysis of final product, in-process, raw material or environmental samples according to Standard Operating Procedures and Test Methods.
• Documentation and review of results in accordance with current Good Manufacturing Practices (cGMP).
• General lab support including housekeeping, equipment maintenance, inventory of supplies, lab supplies ordering, management of glass wares, autoclaving etc.
• Support sample logistics area including retention sample storage, external lab test, QC documents control, shipment of QC samples.
• Prepare, maintain standards and reagents as required by GMP documents.
• Responsible to follow data integrity requirements.
• Problem solving of analytical methods as well as troubleshooting of equipment.
• Involved in equipment qualification, maintenance and troubleshooting.
• Support / Perform OOS, deviation investigations. Draft investigations reports.
• Be a trainer for test method.
• Involvement in method transfers and validation.
• Author Change Controls, Test Methods, SOPs.
• Lead OOS, deviation investigations.
• Assay trend analysis, document revision and update.
• Independently lead and conduct OOS, deviation investigations. Draft investigations reports.
• Support in team leadership.
• Driving results to meet department KPIs.
• Any other duties as assigned by your Supervisor/Manager.

• Degree/Diploma in a relevant Chemistry, Science field or Equivalent discipline.
• Relevant QC testing experience and accomplishment to dictate final position for which the candidate may qualify.
• Well versed in cGMP regulations.
• Knowledge of area specific to the responsibilities.
• Good problem solving and analytical skills.
• Good communication skills and a key team player.

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.

Reference: R72249

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