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MES Expert with MBR Modeling Expertise

vor 2 Monaten


Burg AG, Schweiz Arcondis Vollzeit
About Arcondis

Arcondis is a global consulting company with a strong focus on the healthcare and life science industries. With a global footprint and offices in North America, APAC, and Europe, we have a unique understanding of the challenges and opportunities in these sectors.

Our mission is to improve the lives of people through our work, and we strive to make a positive impact on the communities we serve. We are owned by a charitable foundation, which drives our commitment to social responsibility and sustainability.

Job Description

We are seeking a highly experienced MES Expert with strong proficiency in MBR modeling in PAS-X (Version 3) to join our team. As a Senior Consultant, you will drive operational efficiency through effective business process management with our clients.

Key Responsibilities
  • Manage and coordinate projects in Manufacturing of Pharma and/or MedTech clients
  • Design and maintain MBRs in PAS-X, preferably Version 3
  • Develop GMBRs based on legacy documentation within given frameworks
  • Develop documentation and conduct user trainings
  • Tightly collaborate with departments like Production, QA, and IT
  • Ensure compliance with GMP, EHS, and SOX guidelines
  • Support hypercare activities
  • Deliver successful consulting and solution engagements with clients, especially:
  • Provide expertise in MES systems
  • Lead implementation and optimization of MES systems
  • Apply LEAN principles to simplify processes
  • Guide the Arcondis team to develop and grow their service portfolio in the Manufacturing and MES area to develop a unique value proposition
  • Develop Arcondis best practices & capability around Manufacturing and MES domain knowhow
  • Drive Business Development within defined industries to grow the business
Requirements
  • A degree in Computer Science, Information Technology, Engineering, or a related field
  • Significant experience with MES WERUM PAS-X and MBR design, including GMBR
  • Pharmaceutical industry experience, especially in MES in Parenterals, Solids, Device Assembly and Packaging, or Fill and Finish
  • Understanding of Regulatory requirements related to Life Sciences manufacturing (GMP, EHS, and SOX)
  • Experience in planning, and/or implementing manufacturing digitalization (Industry 4.0)
  • Experience in change management including requirement analysis, design, implementation, review, testing, and documentation
  • Lean Six Sigma / Continuous Improvement certification or related experience is a plus
  • General understanding of Level 3 and 4 systems (e.g. SAP, MES, PCS MBR, ANTARES, ATTP)
  • Excellent problemsolving and communication skills
  • English communication skills, written and oral (C1)
  • Good German communication skills (B2)
  • Flexibility and willingness to travel and regularly work at client site