MBRs Design Consutlant

MBRs Design Consultant

Location: Switzerland (hybrid/on-site depending on client needs)

Employment Type: Full-time

Language Requirement: German (mandatory), English (professional)

Salary: Up to 85,000 CHF depending on experience

About the Company

Our client is a leading consultancy specializing in digital transformation and manufacturing solutions for the pharmaceutical and life sciences industry. The team partners with global clients across Switzerland to design, implement, and optimize Manufacturing Execution Systems (MES), ensuring compliance, efficiency, and innovation in regulated environments.

Role Overview

R&D Partners is seeking an experienced Design Consultant with strong expertise to support the design and implementation of MES solutions for pharmaceutical manufacturing clients. You will work closely with cross‑functional teams and Process SMEs to translate business requirements into robust, compliant digital solutions.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities

• Design, configure, and implement Master Batch Records (MBRs) within PAS‑X
• Lead and facilitate process review workshops with Process Subject Matter Experts (SMEs)
• Conduct process design workshops to define future‑state manufacturing workflows
• Translate business and process requirements into MES functional specifications
• Collaborate with stakeholders across Manufacturing, Quality, and IT
• Ensure compliance with GxP regulations and industry best practices
• Support Level 2 (L2) integration topics, including interaction with shop‑floor systems and equipment
• Participate in system testing activities (e.g., FAT, SAT, UAT)
• Provide guidance and support during deployment and go‑live phases
• Contribute to continuous improvement initiatives and digital transformation strategies

Required Skills & Experience

• Proven ability to independently design and develop Master Batch Records (MBRs)
• 2‑3 years of hands‑on experience with Werum PAS‑X MES
• Strong experience facilitating process review and design workshops with SMEs
• Good understanding of ISA‑95 / Level 2 integration concepts
• Experience working in GxP‑regulated environments (pharma, biotech, or life sciences)
• Excellent communication and stakeholder management skills
• Fluent German (spoken and written) – mandatory
• Professional proficiency in English

For more information, please contact Jack Keens.