Ph3Overview /h3pThis job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. /ph3Work Schedule /h3pStandard (Mon-Fri) /ph3Environmental Conditions /h3pOffice /ph3Job Description /h3pAs 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. /ph3Description /h3pJoin our collaborative team as a Regulatory Affairs Specialist I at Thermo Fisher Scientific, where you'll contribute to ensuring our products meet global regulatory requirements and help make the world healthier, cleaner, and safer. You'll 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. /ppAs a valuable member of our Regulatory Affairs team, you'll compile technical documentation, review regulatory requirements, and support product lifecycle management from initial registration through post-market activities. You'll collaborate with Quality Assurance, MSAT, Commercial teams, and regulatory authorities to ensure compliance while facilitating efficient product launches and maintaining existing approvals. /ph3Requirements /h3ulliBachelor's Degree required /liliPreferred Fields of Study: Life Sciences, Chemistry, Pharmacy, Engineering, or related scientific field /liliAdditional qualifications in Quality Management or Regulatory Affairs advantageous /liliExperience with regulatory submissions and documentation management /liliStrong technical writing and documentation skills /liliProficiency in Microsoft Office applications (Word, Excel, PowerPoint) /liliExcellent organizational abilities and attention to detail /liliStrong analytical and problem-solving capabilities /liliEffective verbal and written communication skills in English /liliAbility to work both independently and collaboratively in a matrix environment /liliExperience with regulatory databases and submission systems preferred /liliKnowledge of GMP, ISO 13485, and quality management systems /liliAbility to manage multiple projects and meet deadlines /liliCustomer-focused mindset with strong interpersonal skills /liliDemonstrates company values of Integrity, Intensity, Innovation, and Involvement /li /ul /p #J-18808-Ljbffr