Global Medical Device Regulatory Lead

Resourcing Life Science; Denmark; On-site; DKK 600,000 - 900,000; Full time

Job summary

A leading life science recruitment agency in Denmark is seeking a regulatory affairs specialist with a minimum of 5 years of experience in managing global regulatory submissions for medical devices. The role involves preparing applications and engaging with authorities to ensure timely market access. Strong knowledge of EU regulations is essential. Fluency in English is required. This position offers an opportunity to work with cross-functional teams while ensuring compliance throughout the product lifecycle.

Qualifications

• Minimum 5 years of experience in regulatory affairs or related field.
• Strong knowledge of global regulatory requirements for medical devices.

Responsibilities

• Establish and manage regulatory submission timelines.
• Prepare and file global medical device applications.
• Engage with regulatory authorities for product registrations.

Skills

Regulatory submission management

Fluent English

Job description

A leading life science recruitment agency in Denmark is seeking a regulatory affairs specialist with a minimum of 5 years of experience in managing global regulatory submissions for medical devices. The role involves preparing applications and engaging with authorities to ensure timely market access. Strong knowledge of EU regulations is essential. Fluency in English is required. This position offers an opportunity to work with cross-functional teams while ensuring compliance throughout the product lifecycle.