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Technologist 1, Analytical Method Development and Validation, DS

Salary undisclosed

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Today, Lonza is a global leader in life sciences operating across three 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 to 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.

Did you know that we are the 1st biologics contract manufacturer in ? We offer you exposure to upcoming biotech and established pharmaceutical companies and to the manufacturing technology needed to produce mammalian treatments and cell therapies of tomorrow. Our global manufacturing network is recognized for its reliable, high-quality services, regulatory track record, global footprint, innovative technology platforms and extensive experience – we, in Singapore are proud to be part of this global network

The successful applicant for this position will be joining the Analytical Development team within Development Services in Lonza Singapore, focusing on test method validation, development and life cycle management. The Development Services group is responsible for the development and characterization of manufacturing processes used for the production of novel therapeutic recombinant proteins for Lonza’s global client base. The purpose of this role is to execute analytical work related to the development and validation of purity, impurity, identity or charged isoform analytical methods and to provide technical expertise to support troubleshooting activities in the laboratory to a high standard in compliance with ICH guidelines, GMP and business principles.

The position will be based in Science Park II.

Key responsibilities:

  • Execution of laboratory work supporting analytical testing, method development and method validation on antibodies and other therapeutic recombinant proteins.

  • Test methods employed include, but are not limited to, techniques using capillary electrophoresis, HPLC/UPLC, spectrophotometry, ELISAs, and qPCR.

  • Collaborate within the different functional analytical teams by supporting analytical work for Characterization and Process Analytics, where required.

  • Contribute to customer projects by generating scientific data from experimental work.

  • Support activities that ensure the efficient functioning of the laboratory such as managing inventory, housekeeping and equipment checks.

  • Facilitate communication between other departments in Singapore (e.g. QC/QA/SCM/EHS).

Key requirements:

  • Diploma or Degree (preferred) in a relevant Science field or Equivalent

  • Practical laboratory experience in analytical testing for antibodies or proteins is preferred although training will be provided

  • May suit a candidate with prior experience in a cGMP / QC laboratory.

  • Excellent team working skills

  • Experience working within a formal Quality Management System (cGxP/ISO) is preferred.

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