Location : Lengnau, near Bern. Onsite presence every day is mandatory
Role Overview
We are looking for an experienced Rockwell FTPS MES Consultant to support implementation and enhancement activities at a GMP-regulated biopharmaceutical manufacturing site. The role requires strong hands-on expertise in Rockwell PharmaSuite / FTPS configuration and programming, working closely with manufacturing, quality, and automation teams.
Key Responsibilities
Configure, customize, and support Rockwell FTPS (FactoryTalk PharmaSuite) MES solutions.
Develop and maintain recipes, workflows, and batch configurations.
Perform MES programming and configuration aligned with shop-floor processes.
Support FAT, SAT, IQ, OQ, and validation documentation in GMP environments.
Collaborate with business SMEs, automation, quality, and IT teams.
Ensure compliance with GMP, GAMP5, and 21 CFR Part 11 requirements.
Provide onsite support during implementation, go-live, and stabilization phases.
Required Skills & Experience
6–10 years of experience in MES implementations within pharma / life sciences.
Strong hands-on expertise in Rockwell FTPS / Rockwell PharmaSuite.
Experience with recipe management, configuration, and programming.
Solid understanding of GMP manufacturing processes.
Proven experience in CSV activities (URS, FRS, IQ/OQ).
Excellent communication skills and ability to work in cross-functional teams.
Nice to Have
Prior experience in biologics or bio manufacturing facilities.
Exposure to integrations with PLC/SCADA and ERP systems.
Experience working in European pharma sites, preferably Switzerland.