Regulatory Affairs Specialist Jobs

Dozee·India·Bangalore·On-site

Regulatory Affairs Specialist

Overview: Dozee Health AI is a pioneer in Contactless Remote Patient Monitoring (RPM), proven to drive transformation at scale. Headquartered in Bengaluru, India, Dozee has emerged as India’s no. 1 RPM Company. We are seeking visionary individuals to help us in this very exciting journey. As a part

surescreengroup·United Kingdom·Derby·On-site

Regulatory Affairs Specialist (IVDR) – Fixed Term Contract

SureScreen Diagnostics are an innovative and forward-thinking company creating bespoke diagnostic solutions, products and tailored services for organisations across the UK and Europe for over 30 years. Our mission is to provide the best quality diagnostic products that meet and exceed customers’ exp

lifewave·United States·Draper·On-site

Regulatory Affairs Specialist - EMEA

POSITION SUMMARYRegulatory Affairs Specialist for EMEA region responsible for all things Regulatory in the region, including but not limited to ingredient review, marketing collateral review, product registrations, and label reviews. Understands, implements, and maintains the quality policy. Ensures

singota·United States·Bloomington·On-site

Regulatory Affairs Specialist

careers-benjaminmoore

Regulatory Affairs Specialist

Overview Company Overview At Benjamin Moore, our success is attributable to the employees who dedicate their time and talents to the brand and exemplify our core values of openness, integrity, community, excellence, and safety. Benjamin Moore employees enjoy a competitive and well-rounded benefits p

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freepl·EG·El Manial·On-site

Import & Export Regulatory Affairs Specialist

About the role We are looking for a detail-oriented Regulatory Affairs Specialist to join our operations team at Swift Egypt. This role is the regulatory backbone of our IOR/EOR operation, every medical device and pharmaceutical import that requires an EDA approval, RUI release, or inspection passes

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freepl·EG·Manial·On-site

Regulatory Affairs Specialist

We are part of Swift Group, established in 1991 as Swift Freight by Khaled Morsy, Urs Moll, Mohamed Elwakil, and Amr Yakan. The company quickly gained the trust of global flagship companies as an agent and partner, becoming a market leader and consolidating operations under Swift Group. Since 2016,

expedock·Philippines·On-site

Regulatory Affairs Specialist (Medical Devices & IVD)

About Expedock We are a tech-enabled workforce augmentation platform leveraging top 1% offshore talent & cutting edge technology to enable businesses to unlock their full potential. About the ClientAn established international regulatory affairs and QA consultancy specializing in the medical device

uphill·Portugal·Lisbon·On-site

Regulatory Affairs Specialist – Medical Devices (SaMD)

Location: Lisbon, Portugal (Hybrid options available) About UpHill At UpHill, we’re on a mission to revolutionize healthcare. By developing best-practice clinical pathways and care orchestration software, we help healthcare providers and life sciences companies across Europe streamline their process

DIRECT SALES, US·United States·Marlboro·On-site

Regulatory Affairs Specialist

At Hologic, women's health is at the heart of everything we do. Our Regulatory Affairs team plays a vital role in bringing innovative, compliant, and safe medical technologies to market, helping advance early detection, diagnosis, and treatment solutions that improve the lives of women around the wo

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Hyperfine·United States·Guilford·On-site

Senior Regulatory Affairs Specialist

About Us Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking health technology company that has redefined brain imaging with the Swoop ® system—the first FDA-cleared, portable, ultra-low-field, magnetic resonance brain imaging system capable of providing imaging at multiple points of c

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Hyperfine·United States·Palo Alto·Hybrid

Senior Regulatory Affairs Specialist

About Us Hyperfine, Inc. (Nasdaq: HYPR) is the groundbreaking health technology company that has redefined brain imaging with the Swoop ® system—the first FDA-cleared, portable, ultra-low-field, magnetic resonance brain imaging system capable of providing imaging at multiple points of c

Calyxo·United States·Pleasanton·On-site

Senior Regulatory Affairs Specialist - Pleasanton, CA

Calyxo, Inc. is a medical device company headquartered in Pleasanton, California, USA. The company was founded in 2016 to address the profound need for improved kidney stone treatment. Kidney stone disease is a common, painful condition that consumes vast amounts of healthcare resources each year. O

martiderm·Barcelona HQ, España

Regulatory Affairs Specialist

Regulatory Affairs Specialist 📍 Cervelló (Barcelona) | MartiDerm En MartiDerm llevamos más de 70 años naciendo en la farmacia y desarrollando innovación científica para transformar el cuidado de la piel. Nuestro compromiso con la eficacia demostrada, la ciencia y la innovación nos ha convertido en u

deciphex·United States·On-site

Regulatory Affairs Specialist

Location U.S. based role working from home Limited international travel to Europe as required Regular collaboration with global teams across the U.S., Europe, and Canada About this Role (Responsibilities): This is a remote role with some travel required to global offices. Actively involved with the

scioteq·Belgium·Belgium·On-site

Avionics Regulatory Affairs Specialist

Join and strengthen our growing team in Belgium (Kortrijk) and step into the fascinating world of high-performance visualization solutions for a safer world. We are currently looking for an: Avionics Regulatory Affairs Specialist Are you a proactive and detail-oriented professional with a passion fo

Pivotal·United States·Remote · United States

Regulatory Affairs Specialist

Pivotal is the leader in the emerging market of electric Vertical Takeoff and Landing (eVTOL) aircraft. We design, develop, and manufacture light eVTOL aircraft and are renowned for the BlackFly aircraft the world's first light eVTOL to fly manned missions and enter the consumer market. Efficient, c

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Alimentiv 2·Brazil·São Paulo·Remote · Brazil

Regulatory Affairs Specialist (LATAM)

Responsible for the day-to-day activities and delivery of Global Regulatory Affairs support services. Role will include management of clinical trial applications to Competent Authorities, Ethics Committees and Regulatory Agencies, and the research, review and reporting on applicable global regulatio

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Alimentiv 2·Canada·Toronto·Remote · Canada

Regulatory Affairs Specialist (North America)

Responsible for the day-to-day activities and delivery of Global Regulatory Affairs support services. Role will include management of clinical trial applications to Competent Authorities, Ethics Committees and Regulatory Agencies, and the research, review and reporting on applicable global regulatio

Ōura·United States·Remote · United States

Senior Regulatory Affairs Specialist

Our mission at Oura is to empower every person to own their inner potential. Our award-winning products help our global community gain a deeper knowledge of their readiness, activity, and sleep quality by using their Oura Ring and its connected app. We've helped millions of people understand and imp