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

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profile Job Location:

Lisbon - Portugal

profile Monthly Salary: Not Disclosed
Posted on: 16 hours ago
Vacancies: 1 Vacancy

Job Summary

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team youll 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 worlds 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 youll ensure compliance with global regulations. As a Senior Staff Regulatory Affairs Specialist youll interpret and disseminate global regulations guidelines and emerging industry developments while working with cross-functional teams to bring innovative products to market. Youll 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 Bachelors 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


Required Experience:

Director

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAs part of the Thermo Fisher Scientific team youll 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...
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Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more

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