At a Glance
- Tasks: Lead regulatory strategies and submissions for medical devices in the EMEAP region.
- Company: Join Abbott Laboratories, a leader in healthcare innovation.
- Benefits: Enjoy a competitive salary, healthcare, and flexible benefits.
- Other info: Dynamic team environment with opportunities for professional growth.
- Why this job: Make a real impact in the medical device industry while mentoring future leaders.
- Qualifications: Scientific background and experience in regulatory roles, especially with MDR regulations.
The predicted salary is between 60000 - 80000 £ per year.
Abbott Laboratories in Witney is looking for a Senior Specialist Regulatory Affairs who will lead regulatory strategies and submissions for medical devices in the EMEAP region. The ideal candidate will have a scientific background and experience in regulatory roles, particularly with MDR regulations.
Responsibilities include:
- Engaging with regulatory bodies
- Managing technical documentation
- Mentoring junior team members
Abbott offers a competitive salary and extensive benefits including healthcare and a flexible benefits scheme.
Senior Regulatory Affairs Lead, Medical Devices (EMEAP) in Witney employer: Abbott Laboratories
Abbott Laboratories in Witney is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration in the medical devices sector. Employees benefit from competitive salaries, comprehensive healthcare packages, and a flexible benefits scheme, alongside ample opportunities for professional growth and mentorship within a supportive team environment. Join us to make a meaningful impact in regulatory affairs while advancing your career in a leading global company.
