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TRD Composer Technical Service Specialist (mfd)


Job Location:

Basel - Switzerland

Monthly Salary: Not provided by the employer
Posted: 21 October 2026 (7 days ago)
Application Deadline: 18 January 2027
Vacancies: 1 Vacancy

Job Summary

For our client in the pharmaceutical industry we are looking for a technically skilled professional with proven experience in TRD Composer regulatory documentation and pharmaceutical data management. In this role you will play a key part in the integration and further development of regulatory IT systems while coordinating data governance activities in a highly regulated environment.

Responsibilities
  • Coordinate the implementation of SUAM 3.0 into TRD Composer in collaboration with NVS IT Production
  • Set up the GSRS application and develop interfaces between GSRS and TRD Composer to enable the exchange of substance information
  • Create and maintain the TRD reference data model for substance information
  • Coordinate the TRD Data Governance organization and support consistent data management processes
  • Coordinate technical implementations and system changes with relevant IT and business stakeholders
  • Support change-related activities in accordance with internal IT documentation and change management processes
  • Ensure alignment between technical system requirements and regulatory documentation needs
Requirements
  • Proven hands-on experience with TRD Composer and a thorough understanding of its purpose design and functionality
  • Experience with regulatory processes and documentation requirements in the pharmaceutical industry particularly health authority documentation and/or Good Manufacturing Practice (GMP)
  • Knowledge of IDMP standards and relevant ISO standards including their application in digital processes within a regulated development environment
  • Understanding of IT systems application interfaces data models and data governance
  • Experience working with pharmaceutical substance data; familiarity with GSRS is an advantage
  • Knowledge of IT documentation and change management processes in a regulated pharmaceutical environment
  • Strong technical understanding and the ability to follow programming concepts and system integration requirements
  • Excellent English communication skills with strong coordination stakeholder management and leadership capabilities
Benefits
  • Remote Job
  • 5 weeks of annual leave
  • Coverage of certification costs
  • Reka-Card with a 20% discount on up to CHF 2400
  • CHF 400 contribution towards a fitness membership