Regulatory Affairs Specialist in MedTech
vor 4 Wochen
Become a part of our dynamic organization. At Löwenstein Medical Technology, we pride ourselves on being a mid-sized enterprise within the global Löwenstein Group. Our focus lies in respiratory diagnostics and therapy, where we manufacture top-tier medical products in Germany for worldwide application in sleep and ventilation medicine.
To enhance our Regulatory Affairs division, we are seeking a
Regulatory Affairs Manager for Medical Technology (m/f/d). If you possess a strong commitment to regulatory adherence within the medical sector, this role presents an excellent opportunity for you.
Key Responsibilities:
1. Oversee regulatory submissions and ensure compliance with relevant laws and standards.
2. Collaborate with cross-functional teams to facilitate product development and market access.
3. Monitor regulatory changes and assess their impact on the organization.
4. Provide guidance and training on regulatory requirements to internal stakeholders.
Qualifications:
- Proven experience in regulatory affairs within the medical technology field.
- Strong understanding of regulatory frameworks and compliance processes.
- Excellent communication and interpersonal skills.
Join us in our mission to deliver innovative medical solutions that improve patient outcomes. Your expertise in regulatory affairs will play a crucial role in our success.
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