Analyst, Quality Control at Lonza - Spain

Singapore, , Singapore -

Full Time

Start Date

Immediate

Expiry Date

02 Aug, 26

Salary

0.0

Posted On

04 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

HPLC, Spectroscopy, Empower software, cGMP, Analytical methods, Sample analysis, Equipment qualification, Method validation, Assay trend analysis, Laboratory support, Documentation, Data integrity, Protein concentration, Chromatography, Physiochemical methods

Industry

Pharmaceutical Manufacturing

Description

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. Supports lab operations, sample logistics, and analytical methods (e.g., HPLC, spectroscopy), while contributing to continuous improvement initiatives. 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: 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. Analysis of bulk product, in-process or stability samples, according 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. Any other duties as assigned by your Supervisor/Manager What we are looking for: Degree/Diploma in a relevant Chemistry, Science field or Equivalent. Relevant work experience preferably with Lab experience in a biotech or medically related field. Good understanding of HPLC and Empower software. Provide support in HPLC 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. 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

Perform timely testing and analysis of in-process and final product samples in compliance with cGMP and SOPs. Manage laboratory operations, including equipment maintenance, method validation, and accurate documentation of results.