At a Glance
- Tasks: Support regulatory activities for medical devices throughout their lifecycle.
- Company: Perrigo, a leader in healthcare and medical device innovation.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Join a dynamic team in a fast-paced environment.
- Why this job: Play a vital role in ensuring product compliance and market access.
- Qualifications: Attention to detail and a passion for regulatory affairs.
The predicted salary is between 63000 - 77000 £ per year.
Perrigo is looking for an Associate Professional, Regulatory Affairs within our Medical Device Lifecycle Management team in London. The role supports regulatory activities across the product lifecycle to ensure conformity, documentation compliance, product availability and market access.
You will help with lifecycle management tasks including documentation updates, change assessments, regulatory notifications, registrations/listings and maintaining regulatory records.
Medical Device Regulatory Affairs: Lifecycle Specialist in London employer: Perrigouk
Perrigouk is an exceptional employer that values innovation and collaboration, providing a dynamic work environment in the heart of London. Employees benefit from competitive compensation packages, including bonuses and a company car, alongside opportunities for professional growth through training and development initiatives. With a strong focus on fostering client relationships and enhancing product knowledge, Perrigouk empowers its team to make a meaningful impact in the healthcare sector.
