Senior Regulatory Affairs Lead – EU Pharma/Devices

BD; Grenoble; On-site; EUR 90,000 - 120,000; Full time

Job summary

A leading global medical technology firm is seeking a Senior Regulatory Affairs Specialist to ensure regulatory compliance for its products. The role involves preparing documentation for authorities, contributing to submission strategies, and managing post-market obligations. Applicants should possess a master’s degree and a minimum of 5 years in the pharmaceutical or medical device fields, with strong regulatory knowledge and communication skills.

Qualifications

• Master's degree or higher in life sciences or scientific field required.
• Minimum 5 years of experience in pharmaceutical or medical device industry.
• Strong knowledge of regulatory requirements, especially eCTD submissions.

Responsibilities

• Contribute to international regulatory submission strategies.
• Prepare and submit documentation to authorities for product registration.
• Compile technical dossiers and manage post‑market obligations.

Skills

Regulatory compliance

Regulatory requirements knowledge

Analytical skills

Communication skills

Project management

Fluent English

Education

Master’s degree in life sciences or scientific field

Job description

A leading global medical technology firm is seeking a Senior Regulatory Affairs Specialist to ensure regulatory compliance for its products. The role involves preparing documentation for authorities, contributing to submission strategies, and managing post-market obligations. Applicants should possess a master’s degree and a minimum of 5 years in the pharmaceutical or medical device fields, with strong regulatory knowledge and communication skills.