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Strong fit if you want hands-on MSAT work at a global CDMO and can work on-site in the Portsmouth area supporting commercial-ready biologics processes rather than pure discovery research.
As an MSAT Process Scientist/Engineer II at Lonza, expect tech-transfer and process-support work spanning lab and manufacturing: reviewing batch data, troubleshooting unit operations, writing and updating process documents, and partnering with production, QA, and development so scale-up and commercial runs stay robust and compliant.
Strengthen biologics process fundamentals (upstream/downstream), tech transfer, deviation and CAPA writing, statistical process thinking, and cross-functional communication. No certification list or costs were provided for this role family.
No. The listing is on-site (remote flag is 0) in the Portsmouth area.
Lonza manufactures and develops products and services for pharma, biotech, and nutrition, including custom biopharmaceutical manufacturing.
Manufacturing science and technology: process support, tech transfer, troubleshooting, and documentation that keep commercial processes reliable.
Website: lonza.com/about-lonza/company-profile/locations-worldwide/slough-uk.aspx
Lonza Group AG is a Swiss multinational manufacturing company for the pharmaceutical, biotechnology and nutrition sectors, headquartered in Basel, with major facilities in Europe, North America and South Asia. Lonza was established under that name in the late 19th-century in Switzerland. The company provides product development services to the pharmaceutical and biologic industries, including custom manufacturing of biopharmaceuticals and detection systems and services for the bioscience sector.
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MSAT Process Scientist/Engineer II at Lonza in Portsmouth, Rockingham County About the Role The MSAT Process Scientist/Engineer is responsible for being the primary technical support person for manufacturing processes. This role involves developing a core competency in transferring and supporting processes from first run in plant to PPQ campaigns. Responsibilities Supporting the transfer of processes from development to commercial scale Ensuring process robustness and quality through thorough documentation and validation Collaborating with cross-functional teams including R&D, QA/QC, and manufacturing Identifying and implementing improvements in process efficiency and productivity Providing technical support during production runs to ensure smooth operations What We're Looking For Bachelor's degree in Chemical Engineering, Bioengineering, or a related field (Master’s preferred) Minimum 3 years of experience in process development and/or manufacturing support roles Strong understanding of pharmaceutical manufacturing processes Experience with process validation and documentation Excellent problem-solving skills and ability to work independently or as part of a team Knowledge of regulatory requirements for pharmaceutical manufacturing Working at Lonza Lonza offers relocation assistance for eligible candidates. The company is committed to fostering an inclusive environment where employees can thrive and contribute to the success of the organization. How to Apply To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there. Please ensure all required fields are filled out accurately for a smooth submission process.
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