Manager – Regulatory Affairs, Medical Devices
Dräger
full-time
Posted on:
Location Type: Office
Location: Lübeck • Germany
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About the role
- Achieve effective product approvals and ensure compliance with regulatory requirements
- Develop registration strategies for market entry
- Coordinate the preparation and compilation of documentation for international product approvals
- Continuously update and improve procedures for product approvals
- Exchange information and coordinate with international subsidiaries
- Analyze new regulatory requirements and support their implementation
- Prepare for external audits and inspections
Requirements
- Degree from a university or university of applied sciences in a technical or scientific discipline
- Several years of professional experience in Regulatory Affairs, Quality Management, or Development
- Broad technical understanding
- Analytical skills
- Result-oriented and precise working style
- Committed team player with a strong sense of practical feasibility
- Fluent English skills
Benefits
- Flexible working hours
- Contributions to the company pension plan
- Company sports activities and preventive health courses
- Attractive pay according to the applicable collective agreement, including various additional payments
- Option for remote work
- Individualized onboarding and training
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
regulatory complianceproduct approvalsregistration strategiesdocumentation preparationaudit preparationregulatory analysisquality managementtechnical understandinganalytical skills
Soft Skills
result-orientedprecise working styleteam playerpractical feasibilitycommunication skills
Certifications
degree in technical disciplinedegree in scientific discipline