Regulatory Affairs Specialist

2 days ago


Oslo, Oslo County, Norway TN Norway Full time
Job Overview

We are seeking a Life Sciences Professional to join our QA/RA team. In this role, you will be responsible for ensuring the quality and integrity of our clients' products by reviewing and approving quality documents, conducting internal audits, and participating in supplier assessments.

As a key member of our team, you will have the opportunity to work on complex projects and contribute to the development of new processes and procedures.

  • Main Responsibilities:
  • Ensure compliance with GMP and industry standards through thorough review and approval of quality documents.
  • Identify and address quality issues through effective collaboration with cross-functional teams.
  • Drive process improvements through data analysis and quality metrics.


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