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Your role
You will be joining a global leader in engineering services, working at the heart of the life sciences sector. 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 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 business and technical stakeholders across manufacturing, quality, automation, ERP, validation, and MES teams.
- 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 that may impact modelling quality, delivery timelines, or downstream testing.
- Providing technical guidance and mentoring to other modellers, contributing to modelling standards, quality checks, and reuse strategies.
- Maintaining documentation of design decisions, assumptions, open items, and change history for GMP traceability and auditability.
- Collaborating directly with cross-functional subject matter experts to convert complex requirements into robust, scalable PAS-X configurations.
Your profile
- Minimum of 5 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.
- Solid knowledge of GMP principles, data integrity expectations, and the regulatory context of life sciences manufacturing.
- Experience in sterile, parenteral, packaging, or other regulated manufacturing environments is advantageous.
- Confidence engaging with manufacturing, quality, automation, and validation subject matter experts, and the ability to communicate complex technical concepts clearly.
- Fluency in English and strong on-site engagement skills.
- Strong analytical and root cause analysis skills, attention to detail, and a solutions-focused delivery mindset.
- Experience mentoring or guiding other modellers and contributing to team standards, reuse approaches, and quality practices.
- Experience designing complex gMBRs with multiple process variations or significant operational complexity.
- Experience in large-scale MES deployment programs and familiarity with Körber PAS-X in major life sciences transformation programs is highly desirable.
What you'll love about working here
- Digital campuses and academy: Access more than 60,000 hours of training and digital learning on GenAI, data, and sustainability.
- Worldwide leader of engineering services: Work on programs that help shape how life-saving medicines are manufactured at scale.
- Hybrid working: Employees work with their managers to determine an arrangement that fits their role and personal circumstances.