International Regulatory Affairs Specialist - EMEA (Temporary Contract) - Remote

Overview

The International Regulatory Affairs Specialist will coordinate and track international submissions for IVD products in the EMEA region, ensuring compliance with regulations and assisting in the registration process.

In Short

• Coordinate and track international regulatory submissions.
• Manage daily regulatory blocks and ensure closure.
• Create and implement tools for tracking product changes.
• Collaborate with Global Regulatory Affairs teams.
• Oversee Channel Partner business licenses and renewals.
• Ensure timely registration of IVD products and renewals.
• Work in a collaborative and growth-oriented environment.
• Full-time position with remote work options.
• Independent job with a commitment to work/life balance.
• Opportunity for professional growth in Regulatory Affairs.

Requirements

• University degree in Life-Science/Engineering/Law.
• Significant regulatory experience in IVD/medical devices.
• Strong understanding of regulations and registration requirements.
• Excellent analytical and critical thinking skills.
• Strong organization skills and ability to manage multiple tasks.
• Excellent interpersonal and communication skills in English.
• Ability to collaborate across global teams.
• Ability to drive tasks to completion.

Benefits

• Agilent Result Bonus.
• Stock Purchase Plan.
• Life Insurance and Pension.
• Healthcare benefits.
• Employee Assistance Program.
• Holidays and company activities.
• Commitment to work/life balance.
• Growth opportunities in Regulatory Affairs.