Regulatory Affairs Specialist (0007-0018)

Rockville, MD, US · On site · Posted 1d Leaves the board in 6 days
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Monitor and provide guidance on European Union medical device regulations as the subject matter expert, ensuring device certification process compliance, and coordinating with internal teams to address future developments. Education and Experience Requirements Bachelor’s degree in Pharmaceutical Sciences or related. Special Skills Requirements Two (2) years of experience evaluating European Union Regulatory compliance, analyzing regulatory trends, and managing regulatory affairs projects. Partial Telecommuting is permitted Please copy and paste your resume in the email body (do not send attachments; we cannot open them) and email it to candidates at placementservicesusa.com with job reference #0007-0018 in the subject line. Thank you.