MEDICAL DEVICE REGULATORY AFFAIRS jobs in PENNSYLVANIA, United Kingdom

of education and experience. Prior knowledge of Regulatory Affairs and/or Medical Devices is a plus RAC Certification preferred... Specialist and/or department management. Develop an understanding of global medical device regulations in which the organization...

. Regulatory Affairs Specialist Reference Code US-PAE184-88785 About B. Braun B. Braun Medical Inc., a leader in infusion... and analyzes proposed modifications to drug and device products for regulatory impact. Independently reads, reviews, interprets...

candidate will have prior experience with Regulatory Affairs for IVD device submissions in the context of drugs/biologics.... You will need: Prior experience with Regulatory Affairs for IVD device submissions in the context of drugs/biologics submissions...

's with 2-4 years; Master's degree/PhD 1-2 years medical device regulatory submission experience in the APAC region... and planet through our sustainability efforts. Job Summary: The Regulatory Affairs Specialist (RA Specialist) is responsible...

experience. 5+ years of Medical Device Regulatory Affairs experience, domestic and international. 3 years of experience... technology solutions that make a difference in patients' lives. Position Summary The Sr. Regulatory Affairs Specialist (SRA...

, Global Regulatory Affairs CMC is responsible to oversee and help develop regulatory strategies to support development... Director, Regulatory Affairs CMC is also responsible for the oversight of maintaining and updating CMC sections of submissions...

Advanced Respiratory Technologies, Inc. is a medical device company located outside of Pittsburgh, PA... disease patients. We are seeking a highly motivated and talented individual to join our team as an Senior Medical Device...

and planet through our sustainability efforts. Job Summary: The Principal, Regulatory Affairs, Intelligence, Medical Device... surveillance activities by researching, identifying, and communicating up to date global medical device regulatory requirements...

MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries..., or related experience, Masters or PhD preferred. Minimum of 10 years’ experience in Regulatory Affairs or Strategy or similar...

the impact of Medical Affairs work across the organization. As a Clinical Evidence Planning and Evaluations Manager... Medical Device Regulation (EU MDR) Master’s or PhD in Medical Physics (preferred), Biophysics, Biomedical Engineering...

&D, Marketing, Quality, Regulatory and Clinical Medical Affairs. Drives the application of Design Controls and FDA Human Factors..., quality, regulatory, clinical medical affairs, the strategic marketing team, and business leaders to define detailed designs...

Johnson & Johnson is currently seeking a Manager LCM to join our Medical Device Business Services, Inc. located in West... of publication strategy for selected marketed products in close collaboration with the Medical Affairs team. Prepare and/or manage...

Expertise in US and OUS regulations for medical device advertising and labeling Experience in medical device regulatory affairs..., and medical device use. Ability to handle technical reports, drawings, specifications, regulatory and quality documentation...

finished medical device or related regulated industry with manufacturing processes, operational excellence, quality systems... (US) || Pennsylvania (US-PA) || Center Valley || Quality & Regulatory Affairs (QA/RA)...

Johnson & Johnson is currently seeking a Manager LCM to join our Medical Device Business Services, Inc. located in West... of publication strategy for selected marketed products in close collaboration with the Medical Affairs team. Prepare and/or manage...

finished medical device or related regulated industry with manufacturing processes, operational excellence, quality systems... (US) || Pennsylvania (US-PA) || Center Valley || Quality & Regulatory Affairs (QA/RA)...

of Corrective Action/Preventive Action (CAPA). In conjunction with both the Quality and Regulatory Affairs Departments, drive..., ISO, medical device, etc.) helpful. Mechanical aptitude, machine shop experience or engineering background helpful...