Process Assessment and Validation Scientist II
€48,000 - €67,200 per year
Work Arrangement
Office Days per Week: 4 days
Key Skills
Job Description
Process Assessment & Validation Scientist II
Location: Geleen, Netherlands
Minimum 4 days on Site.
Process Assessment & Validation Scientist II is involved in performing multiple assessments related to the implementation of a new process in the LNL facility, process validation activities and post-TT support of manufacturing processes.
What you will get:
- An agile dynamic working culture
- An inclusive and ethical workplace
- Compensation programs that recognize high performance
- A variety of benefits dependent on role and location. The full list of our global benefits can be also found on https://www.lonza.com/careers/benefits
The full-time annual base pay for this position in The Netherlands is expected to range between EUR 48'000 MIN and EUR 67'200 MAX. Initial salary placement within this range will be determined based on role‑related factors such as experience, qualifications, and expected contribution.
What you will do:
- Execute process assessment and validation activities in close collaboration with internal and external partners, ensuring delivery against agreed project timelines.
- Evaluate all process-related areas—including process design, Aseptic Process Simulation (APS), facility layout, equipment, and materials—from a GMP perspective to identify risks and define effective mitigation strategies.
- Monitor and trend performance data during and post-Technology Transfer (TT), assessing process capability and driving continuous process improvement initiatives.
- Lead root-cause investigations and technical troubleshooting for process-impacting deviations, acting as a Subject Matter Expert (SME).
- Champion and foster a culture of Operational Excellence and continuous improvement across all process activities.
What we are looking for:
- Deep understanding of CGT manufacturing technologies, process assessment, and field advances.
- Practical expertise in Good Manufacturing Practice (GMP) standards, aseptic processing, and Aseptic Process Simulation (APS).
- Proven ability to evaluate process, facility, equipment, and material risks, and implement robust mitigation plans.
- Track record of building strong working relationships with clients and internal cross-functional teams.
- Exceptional written and verbal communication skills, with a commitment to transparency and clarity.
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, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the 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 value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
Core Responsibilities
The scientist will execute process assessment and validation activities, including process design and Aseptic Process Simulation, to ensure GMP compliance. They will also lead root-cause investigations and drive continuous process improvement initiatives post-Technology Transfer.
Requirements
Candidates must possess a deep understanding of CGT manufacturing technologies and practical expertise in GMP standards and aseptic processing. Strong communication skills and the ability to build effective cross-functional relationships are essential for this role.
Benefits
- Agile dynamic working culture
- Inclusive and ethical workplace
- Compensation programs
- Global benefits
About Lonza
Industry: Pharmaceutical Manufacturing
Company size: 10,001+ employees
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.