About this opportunity
CEDENT lists this Global Medical Device Regulatory Strategist opportunity in dallas, Texas. Review the employer’s description below for duties, qualifications and application requirements.
Job description
CEDENT is looking for a Regulatory Affairs Consultant to join their team in Dallas, TX. The role involves developing regulatory strategies for medical devices, ensuring compliance with global standards, and preparing necessary submission documents. The ideal candidate will possess strong communication skills and have experience with FDA and international regulations.
The position requires a minimum of 3 years of experience in regulatory affairs within the medical device sector and a Bachelor’s degree in Life Sciences or Engineering. A proactive approach to problem-solving and the ability to collaborate with cross-functional teams are essential.
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Worksite address
dallas, TX, 75215, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.