Global Regulatory Submissions Coordinator β€” Hybrid in Cirencester

Global Regulatory Submissions Coordinator β€” Hybrid in Cirencester

Cirencester Full-Time 63000 - 77000 Β£ / year (est.) Home office (partial)
Corin Group

At a Glance

  • Tasks: Coordinate global regulatory submissions and collaborate with diverse teams on exciting projects.
  • Company: Corin Group, a leader in medical devices with a focus on innovation.
  • Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
  • Other info: Fast-paced environment with potential for career advancement.
  • Why this job: Join a dynamic team and make a difference in the medical device industry.
  • Qualifications: Strong organisational skills and ability to work collaboratively across functions.

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

Corin Group is seeking a Regulatory Operations Project Coordinator in Cirencester to support global regulatory submissions and cross-functional Regulatory Affairs projects across our medical device portfolio.

Responsibilities include planning, coordinating inputs, and ensuring on-time delivery of regulatory milestones while collaborating with Clinical, Quality, R&D, Product Management, Manufacturing and Supply Chain teams.

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Global Regulatory Submissions Coordinator β€” Hybrid in Cirencester employer: Corin Group

Corin Group is an exceptional employer, offering a dynamic work environment at our global headquarters in Cirencester, where innovation meets quality in orthopaedics. With a strong focus on employee growth, we provide opportunities for professional development, a hybrid working model, and a comprehensive benefits package that includes a generous pension scheme and private medical insurance. Join us to be part of a collaborative team dedicated to making a meaningful impact in the healthcare industry.

Corin Group

Contact Details:

Corin Group Recruitment Team

We think you need these skills to ace Global Regulatory Submissions Coordinator β€” Hybrid in Cirencester

Project Coordination
Regulatory Submissions
Cross-Functional Collaboration
Time Management
Communication Skills
Attention to Detail
Medical Device Knowledge