Aktuelle Jobs im Zusammenhang mit Regulatory Affairs Specialist - Heidenheim an der Brenz, Baden-Württemberg - PAUL HARTMANN AG
-
Regulatory Affairs Specialist
vor 4 Wochen
Giengen an der Brenz, Baden-Württemberg, Deutschland HARTMANN VollzeitWir suchen nach einer Persönlichkeit, die sich für die Zulassung von Medizinprodukten begeistert und Teil unseres Teams wird, das die Sicherheit und Leistungsfähigkeit über den gesamten Produktlebenszyklus sicherstellt. Unterstütze unser Regulatory Affairs Team als Werkstudent (w/m/d) und lerne die entscheidenden Aspekte der Zulassung...
-
Regulatory Affairs Expert
Vor 5 Tagen
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG VollzeitWe are seeking a highly skilled Regulatory Affairs Manager to join our global team at PAUL HARTMANN AG. In this role, you will play a crucial part in ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and safety requirements.Key responsibilities will include:External Service Coordination:...
-
Medical Manager
vor 2 Wochen
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG VollzeitJoin Our Team as a Manager Regulatory Affairs ClinicalWe are Hartmann AG, a global company offering healthcare solutions. As a Manager Regulatory Affairs Clinical you will be an integral part of our team, supporting healthcare professionals with our products and services.About the RoleWe are seeking an experienced professional with a strong background in...
-
Werkstudent Regulatory Affairs
vor 4 Wochen
Giengen an der Brenz, Baden-Württemberg, Deutschland HARTMANN VollzeitWir suchen einen motivierten Werkstudenten (w/m/d) für unser Regulatory Affairs Team. Als Teil unseres Teams wirst du die Sicherheit und Leistungsfähigkeit von Medizinprodukten über den gesamten Produktlebenszyklus sicherstellen.Aufgaben:Unterstützung des Teams in administrativen und organisatorischen TätigkeitenVorbereitung der Erstellung der...
-
Werkstudent Regulatory Affairs
vor 4 Wochen
Giengen an der Brenz, Baden-Württemberg, Deutschland HARTMANN VollzeitWir suchen einen motivierten Werkstudenten (w/m/d) für unser Regulatory Affairs Team. Als Teil unseres Teams wirst du die Sicherheit und Leistungsfähigkeit von Medizinprodukten über den gesamten Produktlebenszyklus sicherstellen.Aufgaben:Unterstützung des Teams in administrativen und organisatorischen TätigkeitenVorbereitung der Erstellung der...
-
Regulatory Affairs Clinical Manager
vor 2 Wochen
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG VollzeitTransforming Healthcare through Regulatory ExcellenceAt PAUL HARTMANN AG, we're committed to helping healthcare professionals deliver the best possible care. As a Clinical Research Manager for Regulatory Affairs, you'll play a vital role in ensuring the proper execution of clinical procedures, guaranteeing medical device compliance with relevant performance...
-
Global Medical Director
vor 4 Wochen
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG VollzeitWe are seeking a highly skilled Global Medical Director - Regulatory Affairs Clinical to join our team at PAUL HARTMANN AG. As a key member of our regulatory affairs team, you will be responsible for ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and safety requirements.Provide and...
-
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG - Karriere VollzeitShape Your Career in Regulatory AffairsAt PAUL HARTMANN AG - Karriere, we're committed to helping healthcare professionals make a positive impact on people's lives. As a Manager Regulatory Affairs Clinical, you'll play a crucial role in ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and...
-
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG - Karriere VollzeitShape Your Career in Regulatory AffairsAt PAUL HARTMANN AG - Karriere, we're committed to helping healthcare professionals make a positive impact on people's lives. As a Manager Regulatory Affairs Clinical, you'll play a crucial role in ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and...
-
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG VollzeitJoin Our Team as a Regulatory Affairs Manager for Post-Market SurveillanceWe are seeking a highly skilled Regulatory Affairs Manager to join our team at PAUL HARTMANN AG. As a key member of our regulatory team, you will be responsible for ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance...
-
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG VollzeitJoin Our Team as a Regulatory Affairs Manager for Post-Market SurveillanceWe are seeking a highly skilled Regulatory Affairs Manager to join our team at PAUL HARTMANN AG. As a key member of our regulatory team, you will be responsible for ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance...
-
Clinical Research Manager for Regulatory Affairs
vor 4 Wochen
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG VollzeitBe Part of a Global TeamWe are looking for a skilled Clinical Research Manager to join our Regulatory Affairs team at PAUL HARTMANN AG. As a key member of our team, you will play a crucial role in ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and safety requirements.Key...
-
Biocompatibility Specialist
vor 1 Monat
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG VollzeitJob Title: Specialist SupportAt PAUL HARTMANN AG, we are seeking a highly skilled Specialist Support to join our team. As a Specialist Support, you will play a crucial role in ensuring the biocompatibility of our medical devices.Responsibilities:Interpret ISO requirements and evaluate outcomes considering device factors, intended use, and scientific...
-
Biocompatibility Specialist
vor 1 Monat
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG VollzeitJob Title: Specialist SupportAt PAUL HARTMANN AG, we are seeking a highly skilled Specialist Support to join our team. As a Specialist Support, you will play a crucial role in ensuring the biocompatibility of our medical devices.Responsibilities:Interpret ISO requirements and evaluate outcomes considering device factors, intended use, and scientific...
-
Biological Evaluation Specialist
vor 4 Wochen
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG - Karriere VollzeitJob Title: Quality Specialist AssuranceAs a Quality Specialist Assurance at PAUL HARTMANN AG, you will play a crucial role in ensuring the quality and safety of our medical devices. Your primary responsibility will be to evaluate the biocompatibility of materials and support product registration, while also contributing to risk analysis and clinical...
-
Biological Evaluation Specialist
vor 4 Wochen
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG - Karriere VollzeitJob Title: Quality Specialist AssuranceAs a Quality Specialist Assurance at PAUL HARTMANN AG, you will play a crucial role in ensuring the quality and safety of our medical devices. Your primary responsibility will be to evaluate the biocompatibility of materials and support product registration, while also contributing to risk analysis and clinical...
-
Waste Management Specialist
vor 2 Monaten
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG VollzeitJob SummaryWe are seeking a highly skilled Waste Management Specialist to join our team at PAUL HARTMANN AG - Karriere. As a key member of our environmental team, you will be responsible for providing expert advice on Health, Safety, and Environmental (HSE) matters, including conducting audits and compliance monitoring.Key ResponsibilitiesEnvironmental...
-
Waste Management Specialist
vor 2 Monaten
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG VollzeitJob SummaryWe are seeking a highly skilled Waste Management Specialist to join our team at PAUL HARTMANN AG - Karriere. As a key member of our environmental team, you will be responsible for providing expert advice on Health, Safety, and Environmental (HSE) matters, including conducting audits and compliance monitoring.Key ResponsibilitiesEnvironmental...
-
Risk Management Specialist
vor 3 Wochen
Biberach an der Riß, Baden-Württemberg, Deutschland GULP – experts united VollzeitCompliance Specialist Job DescriptionAt GULP – experts united, we are seeking a highly skilled Compliance Specialist to join our team. As a Compliance Specialist, you will play a crucial role in ensuring that our company adheres to all relevant laws, regulations, and industry standards.Key Responsibilities:Active participation in the development and...
-
Global Medical Director
vor 2 Monaten
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG - Karriere VollzeitJoin Our Team as a Manager Regulatory Affairs Clinical (f/m/d)We are seeking a highly skilled and experienced Manager Regulatory Affairs Clinical (f/m/d) to join our team at PAUL HARTMANN AG - Karriere. As a key member of our regulatory affairs team, you will be responsible for ensuring the proper execution of procedures demonstrating medical device...
Regulatory Affairs Specialist
vor 2 Monaten
We support healthcare professionals, enabling them to focus on what truly matters: positively impacting people's lives. At PAUL HARTMANN AG, you'll have the opportunity to become part of a global team.
About the RoleAs a Specialist Regulatory Affairs International, you'll be responsible for ensuring the labelling and implementation of products on time according to regulatory requirements. Your tasks will include:
- Global monitoring and improvement of regulatory product documentation and conformity assessments
- Developing proposals to improve the IT infrastructure for the management of regulatory product documentation
Key Requirements:
- Initial professional experience in the medical device environment or another regulatory field of work
- Knowledge and/or experience in the areas of medical devices, technical documentation, and regulatory product documentation, conformity assessment, and post-market surveillance
- A strong interest in and knowledge of electronic regulatory document control and management systems and associated processes
- IT affinity and proficiency with the MS Office package
- Fluent written and spoken German and English
We provide a range of benefits to support your work-life balance and career development:
- International Mobile Working
- Attractive ways of combining work and family life, e.g. childcare subsidy
- 30 days paid leave per year, plus special leave for exceptional life events as well as vacation pay and special annual payment according to collective agreement
- Company pension plan with attractive employer contribution
- Various health and fitness offers, e.g. skin cancer screenings, online courses for mental health, massage offers, yoga during lunch break etc.
- Job Bike Leasing
- Attractive discounts on e.g. travel, fashion, and technology via our corporate benefits platform
Apply now via our online platform.
