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.
Singapore Development Services is responsible for the development and characterization manufacturing processes used for the production of novel therapeutic recombinant proteins for Lonza’s global client base.
Viral Clearance team which is part of Purification department based primarily in Singapore Science Park, works closely with our customers, and with different functions including MSAT, Manufacturing, Regulatory, Proposal/Program Management, Process Development, Supply Chain, Quality Assurance and external testing facility.
As Senior Scientist you will involve in Viral Clearance studies for developmental/IND/BLA programs, performing lab work such as setup & operate chromatography, ultrafiltration and nano-filtration systems in accordance with GMP standards & guidelines (e.g. EMEA and ICH Q5A).
Responsibilities
Strictly adhere to EHS rules and regulations at all times.
Document results in accordance with Lonza policies and current Good Manufacturing Practices (cGMP) – as appropriate.
Perform activities with high levels of Right-First-Time, ensuring flawless execution with individuals training and/or downstream operations.
Lead projects in areas of expertise with growing scale and complexity. Provide mentorship to junior analysts in simpler work stages.
Efficiently plan your own time and prioritize lab work with minimal input from the manager to deliver project goals.
Develop as Dept SME in one or more areas aligned with training plans.
Provide general lab support, including housekeeping, equipment maintenance, and inventory of supplies.
Troubleshoot equipment and scientific issues, developing expertise in resolving project and process-related challenges.
Drive and actively contribute to operational efficiency initiatives.
Participate in internal and customer project teams, communicating directly with customers to ensure project success.
Draft reports/protocols for review and may write SOPs, risk assessments, and related documents for safety and equipment maintenance.
Perform training in areas of expertise and uphold data integrity principles in accordance with Lonza policies. Proactively evaluate, identify, and improve data integrity processes.
Perform any other duties as assigned by Management.
Requirements
Degree/post-graduate degree or equivalent experience in a relevant scientific field.
0 to 4 years of experience in a lab either in industry or academia, or via an industry work training program.
The final role offered will be commensurate with the candidate’s experience.
Proven understanding of the theory and application of antibody production and purification of biological therapeutics.
Solid understanding of cGMP regulations and demonstrate problem-solving and analytical skills.
Excellent communication skills and strong teamworking skills.
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.