Medical Device Regulatory Affairs Associate

Medical Device Regulatory Affairs Associate

Full-Time 63000 - 77000 £ / year (est.) No working from home possible
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At a Glance

  • Tasks: Support regulatory activities for medical devices and ensure compliance across multiple markets.
  • Company: Perrigo Company, a leader in healthcare products with a commitment to quality.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Other info: Gain valuable experience in a fast-paced, collaborative environment.
  • Why this job: Join a dynamic team and make a difference in global healthcare compliance.
  • Qualifications: Interest in regulatory affairs and strong communication skills.

The predicted salary is between 63000 - 77000 £ per year.

Perrigo Company plc in the United Kingdom is seeking a Regulatory Affairs Assistant Professional to support the Medical Device Lifecycle Management team across the product lifecycle. You will assist regulatory activities that help maintain compliance, availability and market access in multiple markets.

Working with cross-functional teams, you will contribute to regulatory documentation, labeling changes, and implementation tracking while building foundational regulatory knowledge in a global context.

Medical Device Regulatory Affairs Associate employer: Perrigo Company plc

Perrigo is an exceptional employer, offering a supportive work culture that values collaboration and professional growth. Located in London, the company provides competitive compensation, flexible hybrid working options, and tailored benefits to ensure employees feel valued both personally and professionally. With a commitment to employee development and recognition as one of America’s Best Employers by State 2024, Perrigo is dedicated to fostering a rewarding environment for its team members.

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Contact Details:

Perrigo Company plc Recruitment Team

We think you need these skills to ace Medical Device Regulatory Affairs Associate

Regulatory Knowledge
Compliance Management
Documentation Skills
Labeling Changes
Market Access Strategies
Cross-Functional Collaboration
Project Tracking