The following responsibilities are awaiting you:
- You prepare and submit applications for conformity assessments and clinical trials involving non-active implantable class III medical devices in the EU.
- You coordinate timely and accurate responses to questions from Notified Bodies and Competent Authorities.
- You compile, assess and update CE technical documentation and clinical trial application dossiers, including documentation provided by third parties.
- You advise cross-functional development teams on quality, analytical, preclinical, and clinical requirements to support the acceptance of regulatory submissions.
- You prepare and maintain product information in accordance with company core data, applicable legislation, and relevant guidelines.
- You manage the regulatory life cycle of CE-marked products, including renewals, change notifications, and annual updates.
- You assess regulatory implications of changes proposed by production sites, marketing teams, and other internal stakeholders.
- You coordinate regulatory projects and collaborate with external partners, including consultants, contract research organizations, and distribution partners.
- You develop regulatory strategies, contribute to cross-functional project teams, and serve as a contact person for regulatory requirements.
- You identify country-specific requirements and manage the submission and maintenance of documentation required in EU countries beyond the CE mark.
- You support additional regulatory activities and responsibilities as required.
What we expect from you:
- You hold a degree in natural sciences, pharmacy, biology, chemistry, engineering (medical devices / bioengineering), or a comparable discipline, ideally at master's or PhD level.
- You bring approximately 1-3 years of professional experience in EU regulatory affairs for medical devices.
- You have a sound understanding of the European regulatory landscape for medical devices.
- You demonstrate strong time management, problem-solving, communication, and digital skills.
- You work independently, remain resilient, and approach challenges with a structured and solution-oriented mindset.
- You collaborate effectively across functions and are able to coordinate projects and influence stakeholders without direct authority.
- You build constructive relationships with internal and external partners, including Notified Bodies and Competent Authorities.
- You communicate fluently and confidently in business English.
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Regulatory Affairs Manager EU in Frankfurt am Main Arbeitgeber: Progressive
Als Arbeitgeber in einem international führenden Biopharma-CDMO-Umfeld bieten wir Ihnen die Möglichkeit, aktiv an der Gestaltung von Qualitätsstrategien mitzuwirken und einen direkten Beitrag zur Versorgung von Patient:innen mit innovativen Biologika zu leisten. Unsere offene und partnerschaftliche Unternehmenskultur fördert die persönliche und berufliche Entwicklung, während modernste Produktionsplattformen und ein starkes Team von Experten Ihnen die Chance geben, Ihre Fähigkeiten in einem dynamischen Umfeld weiter auszubauen.