About this role
Senior Regulatory Affairs Specialist at CooperCompanies. Location: Falmouth or Barcelona or Berlin or Italy or Ballerup or Netherlands or France. Role: leading projects, supporting submissions, conducting assessments Requirements: Master's in pharmaceutical/chemistry/biology, 4+ years regulatory affairs experience (medical device preferred), prior FDA 510(k) and EU MDR experience, MS Office proficiency, strong communication and project skills, fluent English. Category: Legal and Compliance Seniority: Mid Level Tools: Microsoft Office Commitment: Full Time Workplace: Remote Languages: English