job description
Are you ready to join a global biopharmaceutical leader and push the boundaries of modern medicine? GSK is seeking a Senior Biotechnologist 1 to join our innovative manufacturing team. At GSK, we combine cutting-edge science with state-of-the-art technology to deliver life-changing vaccines and medicines to patients worldwide. This role is pivotal in our journey toward 'Smart Manufacturing,' where we harness digital integration and advanced bioprocessing techniques to ensure the highest standards of product quality and efficiency.
As a Senior Biotechnologist, you will be at the forefront of complex biological production. You will work within a collaborative ecosystem of scientists and engineers, operating in an environment that values technical excellence and continuous improvement. We are looking for a visionary professional who understands the nuances of cell culture, purification, and the critical importance of maintaining a sterile, compliant manufacturing environment. This is an opportunity to grow your career in a high-impact setting, contributing to the development of next-generation therapies that address some of the world's most pressing health challenges.
Beyond the technical scope, GSK offers a culture of inclusion and development. We empower our teams to take ownership of their processes and innovate. If you are passionate about biotechnology and driven by a mission to help people do more, feel better, and live longer, we invite you to apply and become a key player in our Bali-based operations.
Responsibility
- Lead and oversee complex upstream and downstream bioprocessing operations, ensuring adherence to production schedules and quality standards.
- Execute and document tech transfer activities and process validation protocols for new biological products.
- Troubleshoot and resolve technical issues related to bioreactors, chromatography systems, and filtration units.
- Maintain 100% compliance with current Good Manufacturing Practices (cGMP), safety guidelines, and environmental regulations.
- Drive continuous improvement initiatives using Lean Six Sigma methodologies to optimize yield and reduce cycle times.
- Mentor and provide technical guidance to junior biotechnologists and technicians to foster a culture of technical excellence.
- Collaborate with the Quality Assurance and Engineering teams to support facility audits and equipment maintenance cycles.
- Analyze process data and author technical reports to support regulatory filings and internal investigations.
Qualifications
- Bachelor’s or Master’s degree in Biotechnology, Biochemistry, Chemical Engineering, or a related life sciences discipline.
- Minimum of 5-8 years of hands-on experience in a large-scale biopharmaceutical manufacturing environment.
- In-depth expertise in mammalian cell culture, microbial fermentation, or protein purification techniques.
- Proven track record of operating in a cGMP-regulated facility with a strong understanding of FDA and EMA standards.
- Experience with automated control systems such as DeltaV, SCADA, or MES.
- Strong analytical and problem-solving skills with the ability to manage complex technical projects.
- Excellent communication and leadership skills, with experience leading cross-functional teams.
- Proficiency in English; knowledge of local regulations is a significant advantage.