required. Minimum ten years of experience in medical device Regulatory Affairs, seven years in medical device Class II/III required. Candidates... with 5+ years of practical experience in the regulated medical device industry may be considered if they possess...
of global regulatory applications, as well as maintenance of internal regulatory file documentation Reviewing device labeling... Required qualifications: Bachelor's degree 3+ years of experience in Regulatory Affairs or related experiences Understanding...
of global regulatory applications, as well as maintenance of internal regulatory file documentation Reviewing device labeling... Required qualifications: Bachelor’s degree 3+ years of experience in Regulatory Affairs or related experiences Understanding...
III Medical Devices Establish the regulatory strategy and global registration plan for products, meeting internal quality.... Minimum of 3 years regulatory affairs experience required with Bachelor's degree. Minimum of 2 years regulatory affairs experience...
experience in regulatory affairs in medical device, biotech, or pharmaceutical industry Experience in regulatory submissions... strategies for new and modified medical devices. Assist in the development of the regulatory strategies for new products...
industry with a minimum of 3 of those years directly related to Class III Medical Devices. Certification... is a plus (such as RAC from the Regulatory Affairs Professionals Society). Ability to work effectively on project teams. Must be able...
years Regulatory Affairs experience in Medical Device regulations. Demonstrated success in taking products through FDA... medical devices in both the U.S. and Europe, support of international product registrations and related regulatory affairs...
of every precision fluid measuring device we manufacture. Responsibilities: Responsible for analysis of new or revised... regulations and standards, communication of regulatory needs to stakeholders and managing cross-functional projects to ensure...
environment, medical device industry or equivalent 4+ Years Experience as a Technician / Scientist or related biological.... Together, we can make an impact! Job Scope The Senior Regulatory Affairs Associate will be responsible for: Individual...
, and customers around the world. You will learn the many aspects of how to be an outstanding regulatory affairs specialist, making... key contributions within the medical device industry. You will learn valuable planning, scheduling, and communication...
) desirable. - RAC desired. 3 skills required for this position 1. Regulatory experience in Medical Device Industry i.e Post... job details: Job Title: Regulatory Affairs Specialist II Location: Chaska MN 55318 Duration:12+ Month Contract Mon-Fri 8 to 5/Flex 7:30 AM...
and category knowledge to US Medical Strategy, Marketing, New Development, US Regulatory Affairs, Communications, Legal and Global..., or Medical Device Industry experience preferred; 5+ years of relevant experience; A thorough knowledge of company policies...
both pre and post-market for medical devices and in vitro diagnostic devices. In addition, the Clinical Affairs Specialist... clinical research, medical writing, clinical science in the medical device and/or pharmaceutical industry Familiarity...
both pre and post-market for medical devices and in vitro diagnostic devices. In addition, the Clinical Affairs Specialist... clinical research, medical writing, clinical science in the medical device and/or pharmaceutical industry Familiarity...
- To Improve the Quality of Life for Women! As a regulatory specialist, you will develop and implement medical device regulatory...). Regulatory Affairs Certification (RAC). Who is Caldera Medical? Caldera Medical is a growth stage medical device company...
, Permanent Position: Senior Regulatory Specialist- Hybrid 3 days on-site and 2 days remote. Company Overview...: We are seeking an experienced Senior Regulatory Specialist to join our team. The Senior Regulatory Specialist will be responsible...
) within the medical device, pharmaceutical or health care industry Preferred Qualifications: Degree or work experience in... Regulatory Affairs Operations team is looking for a dynamic, well-organized individual who can be a contributing member...
) within the medical device, pharmaceutical or health care industry Preferred Qualifications: Degree or work experience in... Regulatory Affairs Operations team is looking for a dynamic, well-organized individual who can be a contributing member...
Specialist, Regulatory Project Management (RPM) role is responsible for management of regulatory affairs projects associated... device development, registration of Class I and Class II, Class III medical devices, and profound knowledge of industry...
’ experience in medical device industry Thorough working knowledge of applicable FDA, ISO, MDR requirements, consensus standards..., and we're committed to attracting and retaining top talent. Job Scope The Regulatory Specialist 2, Business Development...