Senior Regulatory Affairs Strategist – Global MedTech

PharmaJobber; Livingston; Hybrid; GBP 50,000 - 70,000; Full time

Job summary

A leading healthcare company is seeking a Senior Regulatory Affairs Specialist to join their Regulatory Affairs Global Strategy & Implementation team. The candidate should possess a minimum of a bachelor’s degree in science and 3 to 5 years of experience in Regulatory Affairs. Responsibilities include ensuring compliance with regulatory agency regulations and supporting the creation of technical documentation. This full-time, permanent position is based in Livingston, UK offering hybrid working options.

Qualifications

• Minimum of 3 to 5 years of Regulatory Affairs or related experience.
• Experience with healthcare products industry and regulations.
• Working knowledge of EU Medical Device regulatory matters including MDR.

Responsibilities

• Ensure compliance with regulatory agency regulations and interpretations.
• Support regulatory strategies and collaborate with cross-functional teams.
• Support the creation of Technical Documentation for MDR CE marking.

Skills

Regulatory Affairs Compliance

Analytical problem-solving skills

Excellent communication skills

Interpersonal skills

Teamwork

Education

Bachelor’s degree in science or related field

Job description

A leading healthcare company is seeking a Senior Regulatory Affairs Specialist to join their Regulatory Affairs Global Strategy & Implementation team. The candidate should possess a minimum of a bachelor’s degree in science and 3 to 5 years of experience in Regulatory Affairs. Responsibilities include ensuring compliance with regulatory agency regulations and supporting the creation of technical documentation. This full-time, permanent position is based in Livingston, UK offering hybrid working options.