Regulatory Affairs Manager

6 days ago


High Wycombe, Buckinghamshire, United Kingdom Harris Lord Life Sciences Full time £67,500
Job Summary

We are seeking a highly skilled Regulatory Affairs Manager to join our team at Harris Lord Life Sciences. As a key member of our Medical Devices department, you will play a critical role in ensuring the regulatory compliance of our products and services.

Key Responsibilities
  • Lead regulatory and clinical projects, including MDR submissions, new product introductions, and foreign market registrations.
  • Maintain Medical Device Files, support regulatory audits, and provide guidance to cross-functional teams.
  • Collaborate with external consultants, conduct literature reviews, and prepare regulatory documents like Clinical Evaluation and Post Market Surveillance Reports.
  • Develop and implement regulatory strategies to ensure compliance with relevant guidelines and regulations.
  • Provide expert advice on regulatory matters to internal stakeholders and external partners.
Requirements
  • A minimum of 4 years of experience in a Regulatory & Clinical setting within the medical device industry, with a strong focus on technical functions.
  • Degree in law, medicine, pharmacy, engineering, or another relevant scientific discipline.
  • Proven experience in line management and task delegation.
  • Excellent writing and communication skills, with the ability to prepare high-quality regulatory documents.
  • Strong knowledge of clinical evaluation guidelines and regulations, including MEDDEV 2.
What We Offer
  • A competitive salary and benefits package.
  • Ongoing training and development opportunities to support your career growth.
  • A collaborative and dynamic work environment.
  • The opportunity to work on high-profile projects and make a significant impact in the medical device industry.


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