Associate Director, Regulatory Affairs - Clinical Trials (FSP Strategy & Business Development) (Madrid)

Associate Director, Regulatory Affairs - Clinical Trials (FSP Strategy & Business Development) (Madrid)

04 oct
|
ThermoFisher Scientific
|
Madrid

04 oct

ThermoFisher Scientific

Madrid

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION

Join our Regulatory Affairs team at Thermo Fisher Scientific, where you'll ensure compliance with global regulations. As a Senior Staff Regulatory Affairs Specialist, you'll interpret and disseminate general regulations, guidelines, and emerging industry developments while working with cross-functional teams to bring innovative products to market. You'll contribute to developing and implementing regulatory strategies, maintain compliance throughout product lifecycles, and support continuous improvement of our regulatory tools and information systems.

This role offers the opportunity to make a meaningful impact by supporting patient safety while enabling business growth through effective regulatory compliance.

REQUIREMENTS

Advanced Degree plus 6 years of regulatory affairs experience,



or Bachelor's Degree plus 8 years of regulatory affairs experience

Preferred Fields of Study: science, engineering, pharmacy, or related field

In-depth knowledge of global regulatory requirements and frameworks, particularly relating to emerging technologies

Proven track record in regulatory submissions and filings with global authorities

Strong ability to evaluate regulatory impact on products and provide strategic recommendations

Experience managing and improving regulatory information systems (RIMS)

Expert communication and presentation skills for conveying complex regulatory concepts

Advanced project management capabilities to handle multiple complex initiatives

Demonstrated ability to collaborate and engage with key stakeholders

Experience liaising with regulatory authorities, trade associations, and professional bodies

Proficiency with regulatory software tools and systems

Ability to develop regulatory policies and guidelines

Experience in post-market surveillance and vigilance activities

Strong cross-functional collaboration skills

Ability to work effectively in a global environment

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

📌 Associate Director, Regulatory Affairs - Clinical Trials (FSP Strategy & Business Development) (Madrid)
🏢 ThermoFisher Scientific
📍 Madrid

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