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ThermoFisher Scientific Regulatory Affairs Specialist II in Singapore, Singapore

Job Description

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work. Surrounded by collaborative colleagues, you’ll have the support and opportunities that only a global leader can give you. Our respected, growing organization has an outstanding strategy for the near term and beyond. Take your place on our strong team, and help us make significant contributions to the world.

Job Description:

As a Regulatory Affairs Specialist within the Genetic Science Division (GSD) and Clinical Next-Generation Sequencing Division (CSD), you will play important role in impacting patient's life and improve global health outcome. Your expertise will contribute in maintaining the regulatory compliance of the organisation and ensuring our product meets the relevant regulatory requirements.

Tasks and Functions:

  • Partner with global, regional and local team members to ensure timely product registrations in SEA region.

  • Prepare accurate submission dossier based on CSDT, or other relevant formats.

  • Ensure license are maintained in accordance with commercial needs. Tasks includes re-registration, renewal, amendment, change notification, etc.

  • Report MDR/ Adverse Event/FSCA/Recall to regulatory authorities, if needed.

  • Review labelling and promotional materials for regulatory compliance.

  • Ensure the registration records and database are properly maintained.

  • Support regulatory intelligence related assignment.

  • Adhere to procedures to ensure compliance with ISO 13485, MDSAP, US FDA, IVDR, and ISO 9001 standards.

  • Handle other works assigned by supervisor.

Education and qualification

  • Bachelor’s degree or higher degree in Engineering, Sciences, or comparable field.

  • Minimum 4 years of meaningful experience in regulatory affairs related to In Vitro Diagnostic (IVD) Devices and/or Medical Devices.

Knowledge, Skills, Abilities

  • In-depth knowledge in IVD/medical devices regulations, standards and guidelines in SEA.

  • Excellent communication, written, verbal and presentation skills, particularly in regulatory affair applications.

  • Ability to work effectively across cultures and functions.

  • Strong analytical skills and attention to details.

  • Systematic in handling multiple registration work.

  • Able to work under pressure and flexible working hours based on business requirements.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Apply today! http://jobs.thermofisher.com

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.

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