Regulatory Project Manager

il y a 1 semaine


Gidy, Centre-Val de Loire, France PQE Group Temps plein

About PQE Group

PQE Group is a world leader in the Pharmaceutical and Medical Device industries, with a strong presence in Europe, Asia, and the Americas. Our company has been at the forefront of these industries since 1998, with a network of 40 subsidiaries and over 2000 employees.

Job Summary

We are seeking a highly experienced Compliance Qualification & Validation Project Manager to support our projects in France. The successful candidate will be responsible for developing processes and procedures to meet regulatory requirements and industry standards.

Key Responsibilities

  • Develop and implement Qualification/Validation processes and procedures
  • Review and improve existing Qualification/Validation processes
  • Ensure compliance with regulatory requirements and industry standards
  • Collaborate with cross-functional teams to achieve project goals
  • Provide guidance and support to team members on Qualification/Validation matters

Requirements

  • 5+ years of experience in Qualification/Validation in a Pharmaceutical context
  • Strong knowledge of regulatory requirements and industry standards
  • Excellent communication and project management skills
  • Fluent English language skills, with the ability to draft documents in French-English
  • Experience in Validation in the field of experimental drugs is a plus

About the Role

This is an exciting opportunity to work on international projects, develop your skills, and interact with colleagues from around the world. If you are a motivated and experienced professional looking to take your career to the next level, we encourage you to apply.


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