At a Glance
- Tasks: Support lifecycle regulatory activities for medical devices and manage technical documentation.
- Company: Perrigo Company plc, a leader in healthcare innovation.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Gain expertise in a fast-paced, global environment.
- Why this job: Join a dynamic team and make a difference in global healthcare.
- Qualifications: Interest in regulatory affairs and strong collaboration skills.
The predicted salary is between 63000 - 77000 £ per year.
Perrigo Company plc is seeking an Associate Professional, Regulatory Affairs to support lifecycle regulatory activities for our medical device portfolio across markets. You will help manage technical documentation, regulatory records, and labeling updates under guidance within a dynamic global environment.
You will collaborate with Quality, R&D, Supply Chain, Manufacturing and Regulatory Operations to ensure conformity and timely regulatory deliverables, while developing expertise in medical.
Medical Device Regulatory Affairs – Lifecycle Specialist 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.
