MES Expert – Business Analyst – 6244 URA

 

Our client is a pioneer in Drug Discovery and Development and one of the frontrunners in Personalised Healthcare. As the world`s largest R&D spender in the pharmaceutical and diagnostics domain, they work in a vast number of drug discovery & therapeutic areas and are highly recognized internationally.

 

The Synthetic Molecule Factory (SMF) Project in Basel aims to build up new facilities for the production of synthetic molecules by replacing the currently used facilities, refurbishing Building 50, and constructing a new Building 51 with 11 new production lines for the production of APIs.

As part of this project a MES system shall be put in place to bring the factory from a paper-based process to a fully integrated paper-less process including review-by-exception, and a state-of-the-art digitalization.

 

The project is at the point to start discussing and describing full E2E processes. Our client is looking for a strong Senior MES Expert with proven Business Analyst capabilities, able to analyse, discuss and describe business processes. He/she should be able to provide guidance in best practices for MES processes in a gxp-relevant pharmaceutical environment. A good candidate should be able to establish a good working relationship with business stakeholders and is able to organize and lead workshops.

 

The perfect candidate has minimum 10 years of experience with MES systems and MES processes. Additionally we are looking for someone with proven experience in MES manufacturing processes and expertise at least in one MES product from Siemens, Tulip, and/or Rockwell.

 

This role is a 12 months contract with 60-80% workload and has chances of extension which would eventually increase to 100% and is based in Basel area.

 

Main Responsibilities:

  • Review, refine (also challenge status quo) existing manufacturing process requirements with manufacturing stakeholders; scope is the full E2E processes.
  • Simplify, harmonize and baseline manufacturing process requirements far as possible
  • Align manufacturing process requirements to technical requirements and towards out-of-the-box MES features & functions as far as possible in collaboration with Requirements Engineers and/or MES vendors
  • Ensure GMP/GxP/CSV compliance
  • Organize and lead requirements workshops, align business and IT needs & wants.
  • Collaborates with manufacturing process owners, enterprise and IT solution architects, requirements engineers, systems owners.

 

Qualifications and Experience:

 

·       Relevant working/residency permit or Swiss/EU-Citizenship required

·       Senior MES Expert with Business Analyst capabilities

·       Min. 10+ years of experience with MES systems and MES processes, preferably in the medical device or pharmaceutical industry

·       Has good understanding about top floor and shop floor processes, data models, IT/OT architectures and systems incl. integrations

·       Proven experience in MES manufacturing processes and expertise at least in one MES product from Siemens, Tulip, and/or Rockwell

·       Proves to have excellent understanding on how information flows along manufacturing processes

·       Experience in business partnering, ability to quickly learn new business domains and processes

·       GMP/GxP experience

·       Strong stakeholder management, communication and conflict management skills

·       Analytical, structured, empathic, quality-conscious, target oriented

·       Fluent in English, fluent in German would be a big plus

 

Would you like to learn more about CTC and the opportunity outlined? Please, get in contact with us: you may either use the 'apply now' button, or write an email to us, or reach out to us on the phone.

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