Regulatory Affairs Specialist in Hannover

Regulatory Affairs Specialist in Hannover

Hannover Vollzeit 54000 - 66000 € / Jahr (geschätzt) Hybrid
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Auf einen Blick

  • Aufgaben: Entwickle und unterstütze regulatorische Strategien für innovative Medizinprodukte in EMEA.
  • Unternehmen: Cochlear, ein Unternehmen, das Menschen hilft, zu hören und gehört zu werden.
  • Vorteile: Wettbewerbsfähiges Gehalt, flexible Arbeitszeiten und umfassende Weiterbildungsmöglichkeiten.
  • Weitere Informationen: Moderne Büroumgebung mit regelmäßigen Team-Events und sozialen Initiativen.
  • Warum dieser Job: Mach einen echten Unterschied im Leben von Menschen mit Hörverlust.
  • Qualifikationen: Bachelor-Abschluss in einem relevanten Bereich und 3+ Jahre Erfahrung in Regulatory Affairs.

Das prognostizierte Gehalt liegt zwischen 54000 - 66000 € pro Jahr.

Help Bring Life-Changing Medical Devices to Patients

At Cochlear, our mission is to help people hear and be heard.

Regulatory Affairs plays an essential role in making sure our innovative medical device solutions meet regulatory requirements and can reach the people who need them.

We're looking for an

EU Regulatory Affairs Specialist to help bring innovative medical device solutions to patients across EMEA.

About the Role

Working closely with Regulatory Affairs, Product Development, Clinical Affairs, Quality, and other cross-functional teams, you'll provide regulatory guidance throughout the product lifecycle.

You'll support regulatory strategy, manage submissions to EU Notified Bodies and regulatory authorities, and assess product, labelling, and manufacturing changes.

What You'll Do

  • Develop and support regulatory strategies for products across EMEA
  • Provide regulatory and standards compliance guidance throughout product development
  • Prepare and manage regulatory submissions for new and modified products in the EU and UK
  • Create and maintain technical documentation, product registrations, licences, renewals, and post-approval commitments
  • Assess product, labelling, manufacturing, and promotional changes for regulatory impact
  • Work with Manufacturer Regulatory Affairs, Notified Bodies, regulatory authorities, and cross-functional teams
  • Monitor regulatory changes and support CAPA activities, audits, inspections, and continuous improvement initiatives
  • What You'll Bring
  • Bachelor's degree in a scientific, healthcare, legal, or related discipline
  • 3+ years of experience in Regulatory Affairs, medical devices, product/software development, and/or quality
  • Knowledge of regulatory requirements for medical devices
  • Experience with regulatory submissions and technical documentation
  • Strong communication, documentation, and stakeholder management skills
  • Ability to balance business needs with regulatory requirements and make sound decisions
  • Fluent English, both written and spoken
  • Preferred
  • Master's or doctoral degree in a relevant discipline
  • Regulatory Affairs Certification (RAC)
  • Experience in medical device product or software development
  • Experience working with EU Notified Bodies and regulatory authorities
  • Make a real difference in the lives of people with hearing loss
  • Comprehensive onboarding and product training program
  • Competitive salary, bonus scheme, and annual salary reviews30 days' annual leave plus additional days off on Christmas Eve and New Year's Eve
  • Flexible working hours and hybrid working
  • Employee share plan, Corporate Benefits, childcare support, and sabbatical options
  • Ongoing learning and development opportunities
  • Modern office environment, free parking, and excellent transport links
  • Collaborative culture with regular feedback, team events, sports activities, and social initiatives
  • If you're passionate about

Regulatory Affairs, medical devices, and bringing innovative healthcare solutions to patients , we'd love to hear from you.

  • #Regulatory Affairs #Medical Devices #Healthcare #EMEAJobs #Regulatory #Cochlear Careers

Regulatory Affairs Specialist in Hannover Arbeitgeber: Cochlear

Cochlear ist ein hervorragender Arbeitgeber, der dir die Möglichkeit bietet, einen echten Unterschied im Leben von Menschen mit Hörverlust zu machen. Mit einem individuell gestalteten Einarbeitungsprogramm, flexiblen Arbeitszeiten und einer partnerschaftlichen Unternehmenskultur fördert Cochlear nicht nur deine berufliche Entwicklung, sondern sorgt auch für ein positives Arbeitsumfeld in Hannover. Zudem profitierst du von attraktiven Sozialleistungen und einem modernen Büro, das eine gute Work-Life-Balance unterstützt.

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Kontaktdaten:

Cochlear Recruiting-Team

Wir glauben, dass du diese Fähigkeiten brauchst, um Regulatory Affairs Specialist in Hannover mit Bravour zu bestehen

Communication Skills
Problem-Solving Skills
Adaptability
Organizational Skills
Flexibility
Compassion
Teamwork