Your role
You will be joining a global leader in engineering services, working at the heart of one of the most exciting and impactful sectors in the world, life sciences. At Capgemini Engineering, we partner with leading pharmaceutical and biotech companies to deliver complex, large-scale manufacturing transformation programs.
We are looking for a Senior PAS-X Modeller to lead the on-site design and configuration of electronic batch records and manufacturing workflows in Körber PAS-X for a major life sciences transformation program. This is a hands-on senior role for a true PAS-X expert who thrives in GMP-regulated environments, enjoys stakeholder collaboration, and takes pride in delivering high-quality, robust MES solutions.
In this role you will play a key role in:
- Leading the end-to-end design and configuration of gMBRs, MBRs, and ESPs in Körber PAS-X, translating approved manufacturing process requirements, batch records, material flows, equipment logic, and quality controls into executable PAS-X designs that meet GMP and data integrity standards.
- Driving and supporting design review sessions, prototype reviews, dry runs, and solution walkthroughs with manufacturing, quality, automation, ERP, validation, and MES stakeholders.
- Configuring and validating PAS-X elements including process steps and sequencing, parameters and calculations, material allocations and flows, equipment references and status logic, exception handling, data collection points, and reusable recipe structures.
- Reviewing source documentation to identify gaps, inconsistencies, or risks and performing technical dry runs to support issue analysis, corrections, and design refinements.
- Providing technical guidance and mentoring to other modellers and contributing to modelling standards, quality checks, and reuse strategies.
- Maintaining documentation of design decisions, assumptions, open items, and change history for traceability and auditability in line with GMP expectations.
- Collaborating directly with cross-functional subject matter experts to convert complex business and process requirements into robust, scalable PAS-X configurations.
Your profile
- Minimum five years of hands-on experience with Körber PAS-X recipe authoring and modelling, with experience delivering electronic batch record solutions in pharmaceutical or biotech manufacturing.
- Deep understanding of gMBRs, MBRs, ESPs, batch execution processes, material flow and BOM logic, equipment modelling, process parameters, and quality controls.
- Strong knowledge of GMP principles, data integrity expectations, and regulated life sciences manufacturing.
- Confidence engaging with manufacturing, quality, automation, and validation teams and communicating complex technical concepts clearly.
- Fluency in English, strong analytical and root cause analysis skills, and a high attention to detail.
- Experience mentoring or guiding modellers and contributing to team standards, reuse approaches, and quality practices.
- Experience designing complex gMBRs and managing PAS-X modelling from initial design through dry run and handover.
What you'll love about working here
- Access to more than 60,000 hours of engineering academy training and digital campuses covering GenAI, data, and sustainability.
- Work on major life sciences programs that help shape how life-saving medicines are manufactured at scale.
- Hybrid working arrangements determined with managers according to role and personal circumstances.