Medical Device Regulatory Affairs Jobs in Mansfield, MA

Shepherd Regulatory Search - Marlborough, MA, United States

approvals to market devices throughout the product development lifecycle while building and managing a regulatory team. Responsibilities: Develop strategies for regulatory approval of medical devices

from: linkedin.com - 14 days ago

Johnson and Johnson - Raynham, MA

Regulations and European Medical Device Regulations (and previous Medical Device Directives) Preferred : • Experience in orthopedics and orthopedic device regulatory requirements. • Experience

from: Johnson and Johnson - 2 days ago

Johnson and Johnson - Raynham, MA

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex...

from: Johnson and Johnson - 2 days ago

Walker Cole International - Boston, MA, United States

. The successful Quality Manager will have: 3+ years of experience in Regulatory Affairs within the Medical Devices Industry Strong working knowledge of Quality Management Systems including ISO13485 requirements

from: linkedin.com - 12 days ago

BostonGene - Waltham, MA, United States

plus years of experience in Regulatory Affairs, including United States and international medical device and/or IVD/CDx regulations. 8 plus years of experience in medical device and/or IVD/CDx industry

from: linkedin.com - 14 days ago

Olympus Corporation of the Americas - Westborough, MA, US

, Regulatory Affairs in obtaining approval to market Olympus medical devices in the markets served by Olympus. Job Duties Facilitate development of regulatory strategy for novel technologies or market segments

from: Olympus Corporation of the Americas - 9 days ago

Olympus Corporation of the Americas - Westborough, MA, US

Required: Regulatory affairs experience in the Medical Device industry is mandatory [minimum 3 years with BS/BA, or 5 years with Associates degree]. Ability to work in small team environment, but also self

from: Olympus Corporation of the Americas - 4 days ago

Withings - Boston, Massachusetts

, as assigned. Requirements Qualifications: Student seeking a Bachelors or Masters degree in regulatory affairs Knowledge in US medical device regulations,21 CFR 820 Quality System Regulation and standards

from: resume-library.com (+1 source) - 16 days ago

Marlborough, MA

with significant regulatory experience, who is willing and able to learn new skills and technologies to ensure the IPG Medical team achieves its mission. The Director of Regulatory Affairs is responsible

from: Pharmadiversityjobboard.com - 8 days ago

Olympus Corporation of the Americas - Westborough, MA, US

Gastroenterology Fellowship Trained Board Certification Minimum of 10 years of biotechnology/pharmaceutical/medical device industry experience in medical affairs, medical technology, medical strategy with experience

from: Olympus Corporation of the Americas (+1 source) - More than 30 days ago