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At Capgemini Invent, we blend strategic, creative, and scientific capabilities to deliver transformation solutions tailored to our clients' challenges. The Intelligent Industry team helps industrial and life sciences clients navigate operational technology, digital manufacturing, and business transformation, delivering smart manufacturing capabilities from strategy through execution.

Tasks

  • Lead client engagements and manage a dedicated team of MES Recipe Authors across multiple projects, ensuring consistent quality, on-time delivery, and adherence to GMP and client-specific standards.
  • Review and approve MBRs, EBRs, and workflow configurations authored by the team, acting as the final content authority before client submission or system go-live.
  • Advise clients on the end-to-end manufacturing systems landscape (MES, DCS, SCADA, ERP, LIMS) and define target architectures that align operational, quality, and IT requirements.
  • Support clients in defining MES roadmaps, platform selection, and implementation strategies, translating business and regulatory requirements into actionable configurations and project plans.
  • Define and continuously improve authoring standards, review frameworks, and best practices for the Recipe Authoring team; build reusable assets and accelerators for use across engagements.
  • Act as a trusted advisor for senior client stakeholders in manufacturing, quality, and IT; lead workshops, design sessions, and steering committee updates.
  • Contribute to proposals, client presentations, and go-to-market positioning of the Intelligent Industry practice; identify expansion opportunities within existing accounts and new clients.

Requirements

  • Educational degree in Engineering, Pharmaceutical Sciences, Chemical Engineering, Information Technology, or a related field.
  • Minimum 5 years of professional experience in management consulting, digital manufacturing, or industrial technology environments, with a strong track record in client-facing roles.
  • Practical experience in MES implementations (e.g., Körber PAS|X, Rockwell FactoryTalk PharmaSuite, Siemens Opcenter) including MBR/EBR authoring, validation support, and go-live activities is strongly recommended.
  • Solid understanding of the broader manufacturing systems landscape: MES in the context of DCS/SCADA, ERP (SAP), LIMS, historian systems, and IT/OT convergence; able to advise clients on cross-system dependencies and integration architectures.
  • Experience leading teams or workstreams, including quality review of deliverables produced by others, with a structured and coaching-oriented leadership approach.
  • Knowledge of GxP regulatory frameworks relevant to Life Sciences manufacturing: FDA 21 CFR Part 11, EU Annex 11, GAMP 5, Computer System Validation (CSV).
  • Consulting acumen: ability to structure complex problems, develop client-ready communications, and contribute to business development and proposal writing.
  • Strong communication and presentation skills in English (written and spoken).
  • German at fluent level is mandatory.
  • Entrepreneurial mindset, client presence, and the drive to build and shape a growing practice area.
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Über uns
Capgemini Suisse SA ist die Schweizer Gesellschaft der internationalen Capgemini-Gruppe und erbringt Dienstleistungen in den Bereichen Technologie, Beratung, digitale Transformation und Engineering. Das Unternehmen unterstützt Unternehmen und Organisationen bei IT-Strategie, Softwareentwicklung, Cloud, Data & AI, Cybersecurity, Business Transformation, Digital Customer Experience und technologischer Umsetzung. Capgemini Schweiz ist an den Standorten Zürich, Basel, Genf und Lausanne präsent und verbindet lokale Beratung mit den Ressourcen und Fachkompetenzen des globalen Capgemini-Netzwerks.
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