Close
Application for:

MBRs Design Consutlant

MBRs Design Consutlant

Reference: BBBH28995
Date posted: 13/04/2026
Job details
Specialism
Engineering
Expertise
Automation Engineer
Location
Basel, Basel-City, Switzerland
Job type
Permanent
Register your interest

If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.

Register interest

Description

Help bring science to life and join a leading pharmaceutical company and play a key role in delivering impactful research that drives healthcare innovation!

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.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.r-dpartners.com/privacy-policy/

Apply for this role
Register your interest

If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.

Register interest

Get in touch

Have questions or need support? Our team is here to help, contact us to discuss your hiring needs or career goals today.

Contact us