- job summary: The Clinical Evaluations Specialist is responsible for managing regulatory documentation related to clinical evaluations, particularly for Medical Device Regulation (MDR) remediation and Post Production Risk Reviews (PPRRs). This role requires strong expertise in clinical literature reviews, regulatory writing, and post-market surveillance activities to support the life cycle management of medical devices. The specialist will serve as a primajob summary: The Clinical Evaluations Specialist is responsible for managing regulatory documentation related to clinical evaluations, particularly for Medical Device Regulation (MDR) remediation and Post Production Risk Reviews (PPRRs). This role requires strong expertise in clinical literature reviews, regulatory writing, and post-market surveillance activities to support the life cycle management of medical devices. The specialist will serve as a prima
- job summary: As a global leader in staffing and recruitment, we are dedicated to connecting you with opportunities that foster growth and advancement in the life sciences sector. Working with a recruiter gives you exclusive access to a vast network of top employers and valuable insights into a wide range of roles. One of our premier partnerships is with a world-renowned leader in eye care, committed to advancing vision health through innovative surgical ajob summary: As a global leader in staffing and recruitment, we are dedicated to connecting you with opportunities that foster growth and advancement in the life sciences sector. Working with a recruiter gives you exclusive access to a vast network of top employers and valuable insights into a wide range of roles. One of our premier partnerships is with a world-renowned leader in eye care, committed to advancing vision health through innovative surgical a
