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Analyst, QC (Product Testing - Shift)

Lonza

As a QC-Analyst you will performs timely testing and analysis of in-process and final product samples in compliance with SOPs and cGMP, ensuring accurate documentation and data integrity.

Access to Lonza’s full suite of employee benefits: www.lonza.com/careers/benefits What you will do: To prioritize and perform the various testing/analysis in timely manner, in order to support the business requirements.

About Lonza

  • What you’ll get An agile career and dynamic working culture in a global life sciences leader.
  • Willing to work 12 hours rotating shift 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.

Responsibilities

  • Supports lab operations, sample logistics, and analytical methods (e.g., HPLC, spectroscopy), while contributing to continuous improvement initiatives.
  • Analysis of bulk product, in-process or stability samples, accordin g to Standard Operating Procedures and Test Methods.
  • Documentation of results in accordance with current Good Manufacturing Practices (cGMP).
  • Problem solving of analytical methods as well as troubleshooting of equipment.
  • Involvement in method transfers and validation.
  • Involved in equipment qualification and technical selection of QC equipment and/or standards and reagents.
  • Assay trend analysis, document revision and update.
  • General lab support including housekeeping, equipment maintenance, inventory of supplies, lab supplies ordering, management of glass wares etc.
  • Good understanding of HPLC, Empower software, Capillary Electrophoresis (CE), TOC, Osmolality, Protein concentration (A280 or SoloVPE) and other physiochemical methods.
  • Provide support in equipment maintenance and qualification.
  • Understanding and execution of spectroscopy, and other assigned methods which may include chromatography methods (HPLC), Protein concentration (A280 or SoloVPE) and other physiochemical methods.

Requirements

  • Any other duties as assigned by your Supervisor/Manager What we are looking for: Degree/Diploma in a relevant Chemistry, Science field or Equivalent.

Preferred

  • Relevant work experience preferably with Lab experience in a biotech or medically related field.

Benefits

  • 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.