Others

Chief Design Control Expert – Medical Devices – 17830

Uppsala, Sweden
Onsite

Huy Tran

HR Administrator

cv@veritaz.se

Job Summary

  • Posted Date

    May 21, 2026

  • Work Type

    Onsite

  • Deadline

    2026-05-25

  • Schedule

    Full-time

  • Location

    Uppsala, Sweden

Job Description

Assignment Description

We are currently looking for a Chief Design Expert

What You Will Work On

  • Execute and maintain Design Control documentation across assigned product portfolios
  • Manage and maintain documentation including DCTM, DHF, Design Inputs/Outputs, specifications, manufacturing descriptions, and justification reports
  • Ensure document governance, version control, and audit readiness
  • Drive post-approval change control execution, including impact assessments and closure activities
  • Support implementation and documentation updates connected to approved Change Controls (CCs), deviations, and CAPAs
  • Maintain and update Risk Management documentation aligned with ISO 14971
  • Perform risk analyses and maintain risk management reports linked to manufacturing and lifecycle activities
  • Provide documentation support and review for regulatory submissions and authority interactions
  • Ensure consistency between design documentation and regulatory filings across EU MDR, US, and Canada
  • Support execution of MDR-related projects and approval activities
  • Contribute technical input to product submissions, manufacturing implementations, and verification initiatives
  • Establish and maintain Life Cycle Management (LCM) documentation packages
  • Ensure specifications remain robust, traceable, scientifically justified, and suitable for regulatory and manufacturing purposes

What You Bring

  • Strong experience working with MDR-related design documentation and design control processes
  • Proven experience maintaining and governing Design Control documentation in regulated environments
  • Deep understanding of EU MDR and global regulatory expectations
  • Experience managing post-approval changes, deviations, and CAPA-related documentation
  • Strong experience with Risk Management processes aligned to ISO 14971
  • Experience supporting regulatory submissions and authority interactions
  • Knowledge of lifecycle management and maintaining compliant documentation structures
  • Experience ensuring specification robustness, traceability, and technical justification
  • Strong documentation, governance, and process management capabilities
  • Ability to collaborate across regulatory, manufacturing, quality, and engineering functions
  • Excellent communication skills with a structured and detail-oriented approach

 

If this sounds interesting please send your CV at cv@veritaz.se

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