Quality Assurance Documentation Specialist

2 weeks ago


Copenhagen, Copenhagen, Denmark Think IT Resources Full time
Job Overview

A Quality Assurance Documentation Specialist is required to provide expertise in GMP, GAMP, and GDP regulations within the pharmaceutical industry.

This role involves collaborating with cross-functional teams to establish and maintain traceability from documented requirements through design documentation to test execution.

Main Responsibilities:
  • Perform technical reviews of test plans and execute practical tests to ensure compliance with regulatory standards.
  • Develop a comprehensive understanding of equipment and FAT/SAT processes to optimize quality assurance procedures.
About the Role:

This is a mid-senior level contract position based onsite in Denmark, requiring strong analytical and problem-solving skills.

Key Requirements:
  • Experience in Pharma documentation and risk assessment to identify potential quality issues.
  • Knowledge of GMP, GAMP, and GDP regulations to ensure compliance and mitigate risks.
  • Strong understanding of equipment and testing processes to develop effective quality control measures.
Benefits:

This role offers a competitive hourly rate in euros and a long-term contract opportunity for professionals seeking career growth.



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