Regulatory Affairs Specialist - Cambridge, MA

Be part of a Regulatory Affairs Team to develop and deploy innovative and compliant regulatory strategies across business and markets to achieve the highest standards for patient safety and product efficacy.In this role you · Assist in the implementation of comprehensive regulato ...

In this role you be part of a Regulatory Affairs Team to develop and deploy innovative and compliant regulatory strategies across business and markets to achieve the highest standards for patient safety and product efficacy. · ...

We are looking for a Regulatory Affairs Specialist to develop and deploy innovative and compliant regulatory strategies across business and markets. · Assist in implementing comprehensive regulatory strategies by collaborating with regulatory subject matter experts (SMEs). · Coor ...

We are seeking a Regulatory Affairs Specialist to support the Life Cycle Management (LCM) Regulatory Affairs team in the creation,maintenance,and review of technical documentation.This role ensures compliance with European and U.S.medical device regulations,includingsuch as EU MD ...

Be part of a Regulatory Affairs Team to develop and deploy innovative and compliant regulatory strategies across business and markets to achieve the highest standards for patient safety and product efficacy. · Assist in the implementation of comprehensive regulatory strategies by ...

We are looking for a Regulatory Affairs Specialist to join our team in Cambridge, MA. In this role you will assist in implementing comprehensive regulatory strategies by collaborating with regulatory subject matter experts (SMEs) to ensure alignment with company objectives and co ...

+Be part of a Regulatory Affairs Team to develop and deploy innovative and compliant regulatory strategies across business and markets to achieve the highest standards for patient safety and product efficacy.+Assist in the implementation of comprehensive regulatory strategies by ...

The Regulatory Affairs Operations (RA Ops) submission group is organized to provide submission development support to project teams and the regulatory community. · ...

This job involves preparing regulatory submissions while ensuring compliance with current regulations. The specialist will maintain meticulous regulatory documentation. · Proficiency in Regulatory Documentation. · Strong understanding of Regulatory Compliance. · ...

We believe there is a smarter, more data-driven way to make decisions in healthcare and our cloud-native AI powered SOPHiA DDM Platform makes that vision a reality on a daily basis.You will have direct input to our mission to democratize data-driven medicine for the ultimate bene ...

We are seeking a Regulatory Affairs Specialist to join our Global Regulatory Affairs Team. The ideal candidate will have experience in regulatory affairs and a passion for driving innovative solutions. · ...

The Regulatory Affairs Specialist US is responsible for preparing and reviewing regulatory submissions and documentation required for U.S. FDA approvals of high-risk medical devices.This position collaborates closely with global Regulatory Affairs colleagues to drive efficient re ...

The Sr. Regulatory Affairs Specialist is responsible for supporting DeepHealth's product and product development and regulatory activities to commercialize new digital products including AI technologies. · ...

The Sr. Regulatory Affairs Specialist is responsible for supporting DeepHealth's product and product development and regulatory activities to commercialize new digital products. · In this role the Sr. Regulatory Specialist will provide regulatory input on design and development a ...

We are a rapidly growing medical technology company using AI to enable clinicians to make informed decisions on cardiovascular care. · Survey and advance research in cardiovascular CT imaging · , Translate literature and scientific intelligence into meaningful insights · , Develo ...

This individual will be part of the Global Regulatory Affairs team and assists with planning, writing, compilation,and editing of periodic regulatory reports (i.e. DSURs, orphan annual updates,NDA annual reports,PBRERs). · ...

The Credentialing Specialist will support the Office of Professional Staff Affairs at Beth Israel Deaconess Medical Center in Boston. · This role demands exceptional attention to detail and a commitment to high reliability in managing complex privileging requirements across multi ...

The Credentialing Specialist will support the Office of Professional Staff Affairs at Beth Israel Deaconess Medical Center in Boston, · MA.This role ensures accurate,reliable,and compliant credentialing privileging,and peer review processes for medical staff. · ...

+When you join the growing BILH team, you're not just taking a job, you're making a difference in people's lives. · +Ensure accurate and reliable credentialing processes for medical staff. · Support regulatory readiness and data integrity. · +Credentialing & Data Integrity · ...

The Regulatory Affairs Specialist supports the activities of the Regulatory Affairs Department in ensuring compliance with accreditation, licensing, and regulatory requirements. · This position assists with survey readiness, documentation management, · performance tracking, · and ...