Lonza
Analyst 3, QC (Analytical)
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
As a QC Analyst III applies job skills and company's policies and procedures to complete a variety of tasks. The role will encompass a good understanding and execution of spectroscopy, and other assigned methods which may include chromatography methods (HPLC), ELISA, PCR, CE, SDS-PAGE, IEF, TOC, osmolality, potency methods, appearance and other physiochemical methods.
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
To prioritize and perform the various testing/analysis in timely manner, in order to support the business requirements.
Analysis of bulk product 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, autoclaving etc.
What we’re looking for
Degree in a relevant Science field or Equivalent
Minimum 5 years of relevant Lab related experience in a biotech or medically related field
Understanding and execution of ELISA, PCR, potency and FACS methods
Significant years of experience in HPLC / UPLC
Knowledge and Power User of Empower 3
Relevant experience and accomplishment to dictate final position for which the candidate may qualify
Well versed in cGMP regulations
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.