MSAT Downstream Process Scientist I
Lonza
Summary
Join Lonza's Manufacturing Science and Technology (MSAT) team and play a key role in supporting technology transfer and commercial manufacturing activities. This position offers the opportunity to apply scientific and engineering expertise to help deliver life-changing therapies while working in a highly collaborative GMP manufacturing environment.
Job description
What you will do
- Serve as a technical lead for technology transfer and manufacturing process support activities.
- Develop process understanding, perform risk assessments, and support process improvement initiatives.
- Author and review process descriptions, batch records, change controls, and other technical documentation.
- Monitor manufacturing performance, analyze process data, and communicate findings to stakeholders.
- Support deviation investigations, root cause analysis, and product quality assessments.
- Represent MSAT on customer-facing and internal project teams, including audits and operational meetings.
- Support lot release activities and ensure compliance with cGMP and regulatory requirements.
What we are looking for
- Bachelor's degree in Biological Sciences, Biomedical Engineering, Chemical Engineering, or a related scientific discipline.
- Master's degree or PhD preferred.
- Experience supporting manufacturing processes, technology transfer, or process development activities.
- Knowledge of GMP-regulated manufacturing environments.
- Strong analytical, problem-solving, and data interpretation skills.
- Experience authoring and reviewing technical documentation.
- Effective communication and collaboration skills with cross-functional teams.
Requirements
- Bachelor's degree in Biological Sciences, Biomedical Engineering, Chemical Engineering, or a related scientific discipline
- Master's degree or PhD preferred
- Experience supporting manufacturing processes, technology transfer, or process development activities
- Knowledge of GMP-regulated manufacturing environments
- Strong analytical, problem-solving, and data interpretation skills
- Experience authoring and reviewing technical documentation
- Effective communication and collaboration skills with cross-functional teams
Benefits
- Medical, Dental & Vision
- Professional Development
- Compensation Programs
Company overview
Lonza is a pioneering global Contract Development and Manufacturing Organization (CDMO) and a world leader in pharmaceutical manufacturing services. Founded in 1897 in Switzerland, the company has evolved into the first and original CDMO, now operating as one of the largest Western CDMO networks with approximately 19,000 employees across more than 30 sites spanning five continents. Lonza specializes in transforming therapeutic discoveries into life-saving and life-enhancing treatments for patients worldwide. The company's comprehensive services span from early development to drug substance and drug product manufacturing, covering established and emerging technologies including mammalian biologics, small molecules, highly potent APIs, bioconjugates, mRNA, microbial products, and cell and gene therapies. With a focus on cutting-edge science, smart technology, and lean manufacturing, Lonza serves a diverse customer base ranging from emerging biotechs to global pharmaceutical companies, delivering integrated solutions throughout the entire treatment lifecycle.