Regulatory Analyst - Clinical Affairs

Regulatory Labeling Analyst with 4 years in the medical device industry, specializing in EU MDR 2017/745 compliance, DHF remediation, labeling gap assessments, and verification protocols and reports. Proven track record in project planning, execution and leading cross-functional teams and improving label productivity by 100%. Proficient in tools likeTeamCenter and Adobe Acrobat pro with strong documentation and stakeholder collaboration skills.