
Senior Medical Device Compliance Officer
2 weeks ago
We are seeking a highly skilled Regulatory Affairs Specialist to join our team.
Main Responsibilities:- To ensure compliance with all relevant regulations and standards in the medical device industry.
- To develop and execute regulatory strategies for product registration, approval, and compliance.
- To manage day-to-day regulatory activities, including submissions, reviews, and approvals.
- Bachelor's degree in Engineering or Science.
- At least 6 years of experience in regulatory affairs within the medical device industry.
- Strong knowledge of ISO 13485, ISO 14971, EU MDR, UK MDR, MDSAP, and US FDA regulations.
This role offers excellent opportunities for career growth and professional development. You will be working as part of an interdisciplinary team to drive innovation and success.
What We Offer:- A competitive salary and benefits package.
- A comprehensive training program to enhance your skills and knowledge.
- The opportunity to work on challenging projects that contribute to the company's success.
We are a leading company in the medical device industry, dedicated to developing innovative solutions that improve patient outcomes.
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