Associate Director, Regulatory Affairs – Clinical Trials (Santiago de Compostela)

Associate Director, Regulatory Affairs – Clinical Trials (Santiago de Compostela)

03 oct
|
ThermoFisher Scientific
|
Santiago de Compostela

03 oct

ThermoFisher Scientific

Santiago de Compostela

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAs 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 global 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 experiencePreferred Fields of Study: science, engineering, pharmacy, or related fieldIn-depth knowledge of integral regulatory requirements and frameworks, particularly relating to emerging technologiesProven track record in regulatory submissions and filings with global authoritiesStrong ability to evaluate regulatory impact on products and provide strategic recommendationsExperience managing and improving regulatory information systems (RIMS)Expert communication and presentation skills for conveying complex regulatory conceptsAdvanced project management capabilities to handle multiple complex initiativesDemonstrated ability to collaborate and engage with key stakeholdersExperience liaising with regulatory authorities, trade associations, and professional bodiesProficiency with regulatory software tools and systemsAbility to develop regulatory policies and guidelinesExperience in post-market surveillance and vigilance activitiesStrong cross-functional collaboration skillsAbility to work effectively in a global environmentThermo 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.#J-18808-Ljbffr

📌 Associate Director, Regulatory Affairs – Clinical Trials (Santiago de Compostela)
🏢 ThermoFisher Scientific
📍 Santiago de Compostela

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