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Singapore, Singapore
Onsite
The QA Specialist will support day-to-day Quality Assurance activities in accordance with approved SOPs / Policies for a multi-product, cGxP contract manufacturing facility
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. Learn new skills and capabilities. 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.
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’ll do
Identify cGxP/cGDP non-compliance, provide guidance, and support basic compliance queries across departments.
Review batch records and logbooks, raise deviations, compile lot genealogy, and prepare lot disposition packages to ensure timely product release.
Oversee product status, shipping documentation, material release, joint inspections, and quality tag-out processes.
Participate in deviation investigations using RCA tools and ensure timely CAPA implementation and closure.
Provide QA oversight for document changes, changeovers, and Quality Change Requests.
Conduct shopfloor walkdowns, escalate process events per SOPs, and support regulatory and customer audits.
Lead or support QA projects and build strong working relationships with internal and external stakeholders.
Demonstrate effective problem-solving skills, data analysis, and strong interpersonal collaboration.
Any other tasks as and when assigned by supervisor
Willingness to work in a rotating 12-hour shift pattern.
What we’re looking for
Degree in science or related field
Relevant work experience in Pharmaceutical Manufacturing industry or Validation / Quality unit in the Biopharmaceutical industry
Familiar with Regulatory requirements and local Codes & Standards (e.g., FDA, EMEA, and ICHQ7)
Knowledge and experience of the practical and theoretical requirement of quality management system in GMP facility
Team player who can operate independently, with strong focus on safety, quality and timelines
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.