Regulatory Affairs Specialist

Work Schedule

Environmental Conditions

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 collaborative team as a Regulatory Affairs Specialist I at Thermo Fisher Scientific where youll contribute to ensuring our products meet global regulatory requirements and help make the world healthier cleaner and safer. Youll work with cross-functional teams to manage product registrations maintain compliance documentation and support regulatory submissions across international markets. This position offers excellent professional development opportunities within our innovative environment focused on serving science.

As a valuable member of our European Regulatory Affairs team youll compile technical documentation review regulatory requirements and support product lifecycle management from initial registration through post-market activities. You will collect and manage data about chemicals and the CLP classification. You will collaborate with business development and procurement teams to align compliance considerations with strategic goals for portfolio expansion.

You will collaborate with Commercial teams Customer Service Suppliers Quality Assurance and regulatory authorities to ensure compliance while facilitating efficient product launches and maintaining existing approvals.

REQUIREMENTS:
Bachelors Degree required no prior experience required
Preferred Fields of Study: Life Sciences Chemistry Pharmacy Engineering or related scientific field
Additional qualifications in Quality Management or Regulatory Affairs advantageous
Knowledge of medical device and IVD regulations (EU MDR/IVDR FDA international requirements)
Experience with regulatory submissions and documentation management
Strong technical writing and documentation skills
Proficiency in Microsoft Office applications (Word Excel PowerPoint)
Excellent organizational abilities and attention to detail
Strong analytical and problem-solving capabilities
Effective verbal and written communication skills in English
Ability to work both independently and collaboratively in a matrix environment
Experience with regulatory databases and submission systems preferred
Knowledge of GMP ISO 13485 and quality management systems
Ability to manage multiple projects and meet deadlines
Customer-focused mindset with strong interpersonal skills
Demonstrates company values of Integrity Intensity Innovation and Involvement