MES Consultant
Company
Global digital manufacturing consultancy specialising in LIMS and MES. Their expert teams support leading life science and pharmaceutical organisations in modernising and digitalising operations- from process design and system implementation to validation and hyper‑care support.
The Role
We’re looking for an MES Consultant with strong experience in Pharma/GMP‑regulated environments. You’ll work with major life science clients to improve manufacturing processes, lead MES implementation workstreams, and support system integrations across complex IT landscapes.
Key Responsibilities:
Support and lead MES project delivery, from requirements gathering through to configuration, testing and go‑live
Analyse manufacturing processes and identify optimisation opportunities within GMP environments
Translate business requirements into actionable technical plans
Work across MES, ERP and automation integrations
Produce documentation, training materials and ensure alignment with regulatory standards (FDA, GAMP5)
Requirements:
Strong experience working in GMP or pharmaceutical manufacturing environments
Hands‑on experience with any recognised MES platform (e.g., PharmaSuite, PAS‑X, Syncade, Opcenter, Infor, etc.)
Professional fluency in German (B2+)
Hybrid on-site requirement near Basel, Switzerland
What’s on Offer:
Full‑time, permanent position with a fast‑growing digital manufacturing consultancy
Strong career progression, visibility and professional development
Training on Pharmasuite MES provided.