After an onboarding period in Visp, Switzerland, the position will be based in the U.S (East or Mid-West Coast) to support the expansion of small molecules/bioconjugation capabilities. Relocation targeted in Q1 2027 and assistance is available for eligible candidates and their families, if needed.
Whatyouwillget
An agile career and dynamic working culture, with the opportunity to work on an international assignment
A highly collaborative environment that fosters teamwork and inclusion
A range of professional development programs to grow your skills and career
An ethical workplace where tasks are carried outin accordance withrelevant procedures
The full list of our global benefits can be also found onhttps://www.lonza.com/careers/benefits
Whatyouwill do:
As the MSAT Process Lead, you will define and drive process technology strategy for a new pharmaceutical manufacturing facility. You will play a key role in facility design, technologyselection, and startup, ensuring scalable, efficient, and GMP-compliant manufacturing processes.
Define and support process technology strategy aligned with product and facility needs
Leadselectionand implementation of process equipment and process analytical technology (PAT)
Collaborate with internal teams and customers to understand product requirements, including critical quality attributes (CQAs), process parameters, and scale-up considerations
Develop production models (throughput, cycle times, capacity) to support facility design and operational planning
Evaluate and recommend technology solutions, balancing performance, cost, flexibility, and compliance
Provide technical input into user requirement specifications (URS), process flow diagrams, and equipment layouts
Partner with automation and OT teams to integrate process control and PAT strategies
Support commissioning and qualification activities, including FAT and SAT
Interface with stakeholders throughout design, construction, and startup phases
What we are looking for:
8+ years of experience in MSAT, process engineering, or technical operations within a GMP-regulated pharmaceutical or biotech environment
Bachelor’s degree in chemical engineering, Bioprocess Engineering, or related fieldrequired; advanced degree preferred
Strongexpertisein process equipment, PAT, and manufacturing technologies
Experience in bioconjugates and/or advanced synthesis (e.g., complex biologics, ADCs, or small molecule processes)
Proven ability to translate product requirements into scalable manufacturing solutions
Experience supporting facility startup, commissioning, and tech transfer
Strong analytical and problem-solving skills, including productionmodelingand process evaluation
Familiarity with automation systems, process control strategies, and data integrity principles
Excellent communication and stakeholder management skills, including customer-facing experience
Collaborative mindset with the ability to work across functions and influence decision-making
Travel: Willingness and ability to travel to EMEA and NA atapproximately 20% of the time to meet business objectives
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence,PassionandIntegrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, andthat’sthe kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion,color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. Ifyou’reready to help turn our customers’ breakthrough ideas intoviabletherapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences?Applynow

Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.
Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.
For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.