Scientist 3, Analytical Method Development & Validation, DS

Scientist 3, Analytical Method Development & Validation, DS

Apply locations SG - Tuas Singapore - REMOTE SG - Tuas, Singapore time type Full time posted on Posted Today job requisition id R64445

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 Singapore? 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.

Key responsibilities:

1. Author, review and perform technical review of method development/validation study protocols and reports, ensuring delivery of high quality and GMP-compliant data, where applicable.
2. Execution of laboratory work supporting analytical testing on antibodies and other therapeutic recombinant proteins.
3. Test methods employed include, but are not limited to, techniques using capillary electrophoresis, HPLC/UPLC, spectrophotometry, ELISAs, and qPCR.
4. Experience using Biacore may also be considered advantageous.
5. Collaborate within the different functional analytical teams by contributing to analytical Product Stability and Reference Standard activities, method validation studies and Process Analytics by performing supporting analytical work.
6. Contribute to customer projects by generating and interpreting scientific data from experimental work.
7. Deliver high quality communication to ensure an outstanding customer experience.
8. Working as part of a site and global project team, co-ordinate multiple projects and ensure timely delivery of project work stages.
9. Facilitate communication between other departments in Singapore (e.g. QC/QA) and across the global Lonza network.

Key requirements:

1. Degree in a relevant Science field or Equivalent
2. Practical laboratory experience in analytical testing for antibodies or proteins is required although training will be provided
3. May suit a candidate with prior experience in a cGMP / QC laboratory.
4. Understanding of theory and application of protein production, purification and analysis
5. Excellent problem solving and analytical skills
6. Excellent communication skills (verbal and written)
7. Excellent team working skills
8. Experience working within a formal Quality Management System (cGxP/ISO). The role may require occasional weekend work.

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.