MES Consultant

Job Description – Rockwell FTPS MES Consultant

Start: Immediate / ASAP

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.