Regulatory Project Manager
il y a 1 semaine
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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