At Sentec, we are passionate about advancing patient care through innovative medical technology. We are seeking a Usability and Regulatory Affairs Specialist to play a critical role in ensuring our products are safe, effective, and compliant with global regulations.
In this cross-functional role, you will lead human factors and usability engineering activities while also supporting regulatory submissions and strategy. You will work closely with engineering, clinical, and quality teams to identify and mitigate use-related risksultimately helping bring high-impact medical technologies to market.
Human Factors and Usability:
Regulatory Affairs:
Usability and Regulatory Affairs Specialist • Lincoln, RI, United States
The Director of Imaging leads the medical imaging department by overseeing operations, staff, equipment, and services, ensuring high quality patient care, regulatory compliance and stakeholder sati... Show more
Regulatory CMC Strategy Manager.Partnering closely with global and regional Global Regulatory Affairs colleagues, as well as Global Operations stakeholders, to address regulatory strategy challenge... Show more
Clinical Research Project Coordinator I.The Clinical Research Project Coordinator I provides supervision and non-clinical administrative support for the project.Responsible for initiating and maint... Show more
Regulatory Affairs Specialist Consultant.As a Regulatory Affairs Specialist Consultant you will be responsible for:.Formulate and execute activities associated with regulatory submissions of a nove... Show more
As 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 ... Show more
Summary:The Referral Specialist reports to a Patient Access Supervisor.Under the general supervision, ensures the quality of the referral process is upheld to departmental standards.Evaluates the i... Show more
Determine and document change assessments for US Class II devices to ensure compliance with the US regulation.Plan and prepare submissions for US Class II devices, including creating, translating, ... Show more
Principal Regulatory Affairs Specialist.Regulatory provides regulatory affairs and product development consulting services to enable pharmaceutical, medical and biotechnology companies to obtain re... Show more
Associate Director or Director, Regulatory Affairs (Hybrid 3 Days in Office).The Associate Director or Director of Regulatory Affairs will be a key member of the STAT6 Regulatory team working in pa... Show more
Foreign Disclosure And Policy SpecialistOdyssey Systems has an exciting opportunity for a Foreign Disclosure and Policy Specialist providing support to the Command, Control, Communications, and Bat... Show more
Role:Health Economics SpecialistLocation:Providence, RI- HybridDuration:5 Months contract with possibility of extensions.Hours/Week:35The primary responsibility of the role is to oversee, develop, ... Show more
Director, Global Regulatory Affairs.Bedford, Massachusetts, United States.Stoke Therapeutics is a biotechnology company dedicated to restoring protein expression by harnessing the body's potential ... Show more
Position: Associate Director, Clinical Quality ComplianceLocation: Bedford, MA (On-site 3 days/week)Length: 6 Month ContractPlease no agencies.Direct employees currently authorized to work in the U... Show more
A leading biopharmaceutical solutions organization in Rhode Island is seeking a Senior Medical Editor to ensure compliance with regulatory standards and manage complex medical writing projects.Cand... Show more
Director, Regulatory Affairs - Strategy.Lantheus is headquartered in Bedford, Massachusetts with offices in Canada, and Sweden.For more than 60 years, Lantheus has been instrumental in pioneering t... Show more
Expert Contributor - Chemistry.Task-Based Independent Contractor Opportunity.We're looking for Chemistry experts who can design and solve challenging, real-world reasoning tasks that push the bound... Show more
Location: Providence, RI- Hybrid.Duration: 5 Months contract with possibility of extensions.The primary responsibility of the role is to oversee, develop, and maintain the Statewide Health Inventor... Show more
CMC Regulatory Affairs Manager.This position is responsible for preparation of CMC submissions for Biologics products.This position will also assist the Regulatory CMC team with special projects as... Show more
Product Testers are wanted to work from home nationwide in the US to fulfill upcoming contracts with national and international companies.We guarantee 15-25 hours per week with an hourly pay of bet... Show more
The Director of Imaging leads the medical imaging department by overseeing operations, staff, equipment, and services, ensuring high quality patient care, regulatory compliance and stakeholder sati... Show more
