Senior Regulatory Affairs Specialist (m/w/d)

Ihre Aufgaben

As a Senior Regulatory Affairs Specialist, you will work closely with all departments and be mainly responsible to prepare / review and maintain the technical documentation as per MDR 2017/745 (EU) and preparation, review and maintenance as well as submissions for international approval.

• Responsible for the creation, review and maintenance of technical documentation
• Responsible for preparation, review and maintenance as well as supporting of submissions for international approval, for re‑registration activities and for the internal communication in view of international regulatory related changes
• Support and guidance of other department for Medical Software and Cybersecurity
• Support Clinical Evaluation, Vigilance / Post‑Marketing Surveillance activities
• Contribution to risk assessments
• Support in the creation and handling of Manufacturer Information (IFU, Labels, Brochure, Website, UDI)
• Support during audit (internal, external, MDSAP, etc.)
• Standard evaluation and administration in the area of expertise
• Support database entries (EUDAMED, DMIDS, GUDID, etc.)
• Ihr Profil
• Appropriate Science or Engineering Degree, preferably in medical technology, or equivalent combination of education and experience in the field of technical documentation and manufacturer information
• At least 5 years of working experience with active / non‑active medical devices (sterile / non‑sterile)
• Fundamental understanding of the new European Medical Device Regulation (MDR 2017/745 (EU))
• Fundamental understanding of ISO medical device standards (ISO 13485, MDSAP, ISO 14971, IEC 60601‑1, IEC 62304, FDA 89 FR 7523, Cybersecurity, etc.)
• Knowledge of regulatory affairs affecting processes (e. g. product
• development, risk management, project management, Vigilance, PMS, CAPA, Complaints, etc.)
• Ability to work under pressure and assertiveness
• Strong team player who is willing to take on and support other activities outside core expertise as required
• Ability to work flexibly across a multi-disciplinary team in jointly achieving given goals
• Able to manage multiple tasks and perform with accuracy and a high attention to detail
• Excellent verbal and written communicator; clear and concise in communications with internal and external partners
• English (C1) and German (B1) language skills, written and spoken
• Time management and organizational skills
• Consistent, quality work and follows through on commitments.
• Basic computer skills (MS Office / MS Visio)

Warum wir?

• Personal induction plan and comprehensive onboarding
• Flexible working hours
• 30 days of holiday
• interesting tasks in a dynamic, international environment
• Continuous training and development
• Flat hierarchies
• Attractive canteen
• Free coffee, tea and water
• Employee events
• Charging stations for electric cars
• Accident insurance
• Employer contribution to VWL
• Employee fund with various allowances and subsidies
• Free language courses
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