Regulatory & Clinical Affairs Pro — Pharma/Devices

Amaris Consulting; Lyon; Hybrid; EUR 60,000 - 90,000; Part time

Benefits offered by this job

Part-time work from home and work from office

Long-term career planning

Professional development plans

Opportunity to bring ideas

Competitive salary

Job summary

A consulting firm is seeking a Regulatory Affairs / Clinical Affairs Specialist in Lyon to manage regulatory projects in pharmaceuticals and medical devices. The role involves advising clients on compliance, preparing regulatory submissions, and monitoring changes in regulations. Candidates should have 5-15 years of experience in regulatory affairs, strong analytical skills, and fluency in English. The position offers part-time remote work, professional development, and competitive salary.

Qualifications

• 5-15 years of experience in regulatory affairs for pharmaceuticals and medical devices.
• Strong analytical and problem-solving skills.
• Fluency in English; French is a plus.

Responsibilities

• Manage regulatory projects in pharmaceuticals and medical devices.
• Prepare and submit regulatory dossiers to competent authorities.
• Advise clients on regulatory compliance and market access.
• Collaborate with multidisciplinary teams to ensure project success.

Skills

Regulatory project management

Regulatory compliance advice

Submission of regulatory dossiers

Monitoring regulatory changes

Analytical skills

Problem-solving skills

Fluent in English

Experience in pharmaceuticals and medical devices

Education

Academic background in Life Sciences, Pharmacy, or Engineering

Tools

Industry-specific tools and software

Job description

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