Global Regulatory Affairs Lead – Medical Devices

Humand Talent; England; On-site; GBP 65,000 - 85,000; Full time

Job summary

A forward-thinking medical device company in the United Kingdom is looking for an experienced Regulatory Affairs Manager. This pivotal role involves managing global regulatory approvals and submissions across established and emerging markets. The successful candidate will work closely with various teams, liaise with regulatory bodies, and shape strategic compliance initiatives to ensure market access for innovative medical technologies. This is a unique opportunity for those looking to make an international impact in the regulatory field.

Qualifications

• Experience in regulatory affairs within the medical device industry.
• Strong understanding of global regulatory requirements.
• Excellent communication skills to liaise with multiple stakeholders.

Responsibilities

• Lead regulatory submissions and renewals across various international markets.
• Act as liaison with regulatory bodies and ensure compliance.
• Contribute to audits and strategic compliance initiatives.

Job description

A forward-thinking medical device company in the United Kingdom is looking for an experienced Regulatory Affairs Manager. This pivotal role involves managing global regulatory approvals and submissions across established and emerging markets. The successful candidate will work closely with various teams, liaise with regulatory bodies, and shape strategic compliance initiatives to ensure market access for innovative medical technologies. This is a unique opportunity for those looking to make an international impact in the regulatory field.