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Senior IT/OT Solution Architect (Pharma Manufacturing)

Confidential · Germany · Hybrid · Senior

  • Germany · Hybrid

Indexed (6 days ago) · refreshed constantly

Start
flexible
Work mode
Hybrid
Contract
Freelance / B2B
Seniority
Senior
Reference
TRCI-26-06219

Required skills

Job description

Senior IT/OT Solution Architect needed for a contract role in Germany (8–12 years) to drive system-level architecture decisions across the IT/OT stack in a pharma/biopharma manufacturing environment. The role covers defining interfaces, data flows and integration specifications; supporting requirements engineering and detailed design documentation; providing

Project overview

Senior IT/OT Solution Architect needed for a contract role in Germany (8–12 years) to drive system-level architecture decisions across the IT/OT stack in a pharma/biopharma manufacturing environment. The role covers defining interfaces, data flows and integration specifications; supporting requirements engineering and detailed design documentation; providing hands-on technical assistance (including source-code components when required); and contributing to testing, qualification/commissioning, hypercare and operational support.

Strong Business–IT–OT collaboration, multi-supplier coordination, GMP/non-GMP awareness, and availability for mandatory on-site qualification/configuration/testing are required. Roche qualification-process knowledge is highly desirable.

Responsibilities

  • Pharma/biopharma industry experience; GMP/non-GMP awareness; effective Business-IT-OT collaboration; multi-supplier coordination; availability for mandatory on-site qualification, configuration and testing activities. Roche qualification-process knowledge is highly desirable.
  • 2 Define system interactions, interfaces, data flows and technical integration specifications.
  • 3 Support requirements engineering and create detailed design documentation.
  • 4 Provide operative technical assistance, including source-code components where required.
  • 5 Support integration across manufacturing, laboratory and automation systems.
  • 6 Contribute technical input to test, qualification, commissioning, hypercare and operational support.
  • 7 Support adaptation of the PTCG IT/OT manufacturing blueprint with other business units.

Requirements

  • Pharma/biopharma industry experience
  • GMP and non-GMP awareness (regulated vs non-regulated environments)
  • IT/OT architecture across manufacturing/lab/automation systems
  • System integration: defining system interactions, interfaces, and data flows
  • Technical integration specifications and detailed design documentation
  • Requirements engineering support (translating requirements into technical design)
  • Hands-on technical assistance, including source-code components when required
  • Support for testing, qualification, commissioning, hypercare, and operational support
  • Business–IT–OT collaboration and stakeholder alignment
  • Multi-supplier/vendor coordination
  • Availability for mandatory on-site qualification, configuration, and testing activities (Germany)

Project details

  • Start: flexible
  • Remote: hybrid
  • Location: Germany, DE

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