Aktuelle Jobs im Zusammenhang mit Director of Global Medical Affairs - Heidenheim an der Brenz, Baden-Württemberg - PAUL HARTMANN AG - Karriere


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG Vollzeit

    We 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 Vollzeit

    Unlock Your Potential in Regulatory AffairsWe are seeking a highly skilled Global Medical Director to join our team at PAUL HARTMANN AG. As a key member of our regulatory affairs team, you will play a crucial role in ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and safety...


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG Vollzeit

    Unlock Your Potential in Regulatory AffairsWe are seeking a highly skilled Global Medical Director to join our team at PAUL HARTMANN AG. As a key member of our regulatory affairs team, you will play a crucial role in ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and safety...


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG - Karriere Vollzeit

    Join 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...


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG - Karriere Vollzeit

    Join 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...


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG Vollzeit

    Job Title: Head of Regulatory Affairs Medical DevicesAt PAUL HARTMANN AG, we're committed to helping healthcare professionals deliver exceptional care. As the Head of Regulatory Affairs Medical Devices, you'll play a crucial role in ensuring our medical devices meet the highest regulatory standards.Responsibilities:Develop and implement regulatory strategies...


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG Vollzeit

    Job Title: Head of Regulatory Affairs Medical DevicesAt PAUL HARTMANN AG, we're committed to helping healthcare professionals deliver exceptional care. As the Head of Regulatory Affairs Medical Devices, you'll play a crucial role in ensuring our medical devices meet the highest regulatory standards.Responsibilities:Develop and implement regulatory strategies...


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG Vollzeit

    Regulatory Affairs ManagerAt PAUL HARTMANN AG, we're committed to helping healthcare professionals make a positive impact on people's lives. We're a company that values innovation, collaboration, and growth. As the Head of Regulatory Affairs, you'll play a key role in driving our regulatory strategy and ensuring compliance with all relevant standards and...


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG Vollzeit

    Regulatory Affairs ManagerAt PAUL HARTMANN AG, we're committed to helping healthcare professionals make a positive impact on people's lives. We're a company that values innovation, collaboration, and growth. As the Head of Regulatory Affairs, you'll play a key role in driving our regulatory strategy and ensuring compliance with all relevant standards and...

  • Medical Manager

    Vor 5 Tagen


    Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG Vollzeit

    Join 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...


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG Vollzeit

    Join Our Team as a Regulatory Affairs ManagerWe are seeking a highly skilled Regulatory Affairs Manager to support our global team in ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and safety requirements.Key Responsibilities:Coordinate external service providers to support clinical...


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG Vollzeit

    Join Our Team as a Regulatory Affairs ManagerWe are seeking a highly skilled Regulatory Affairs Manager to support our global team in ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical performance and safety requirements.Key Responsibilities:Coordinate external service providers to support clinical...


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG Vollzeit

    Join Our Team as a Manager Regulatory Affairs ClinicalWe are seeking a highly skilled and experienced Manager Regulatory Affairs Clinical to join our global team at PAUL HARTMANN AG. As a key member of our regulatory affairs team, you will play a crucial role in ensuring the proper execution of procedures demonstrating medical device compliance with relevant...


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG Vollzeit

    Join Our Team as a Manager Regulatory Affairs ClinicalWe are seeking a highly skilled and experienced Manager Regulatory Affairs Clinical to join our global team at PAUL HARTMANN AG. As a key member of our regulatory affairs team, you will play a crucial role in ensuring the proper execution of procedures demonstrating medical device compliance with relevant...


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG Vollzeit

    Job Title: Regulatory Affairs Manager for Clinical EvaluationAt PAUL HARTMANN AG, we're committed to helping healthcare professionals deliver exceptional care. As a Regulatory Affairs Manager for Clinical Evaluation, you'll play a crucial role in ensuring our medical devices meet the highest standards of safety and performance.Key Responsibilities:Provide...


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG Vollzeit

    Job Title: Regulatory Affairs Manager for Clinical EvaluationAt PAUL HARTMANN AG, we're committed to helping healthcare professionals deliver exceptional care. As a Regulatory Affairs Manager for Clinical Evaluation, you'll play a crucial role in ensuring our medical devices meet the highest standards of safety and performance.Key Responsibilities:Provide...


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG Vollzeit

    Job Title: Clinical Research Manager for Regulatory AffairsWe are seeking a highly skilled Clinical Research Manager for Regulatory Affairs 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...


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG Vollzeit

    Job Title: Clinical Research Manager for Regulatory AffairsWe are seeking a highly skilled Clinical Research Manager for Regulatory Affairs 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...


  • Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG - Karriere Vollzeit

    Shape 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 Vollzeit

    Shape 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...

Director of Global Medical Affairs

vor 3 Monaten


Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG - Karriere Vollzeit

About the Role:

At PAUL HARTMANN AG, we empower healthcare professionals to concentrate on their core mission: enhancing the quality of life for individuals. As a Global Medical Director, you will play a pivotal role in our international operations, ensuring that our medical devices meet the highest standards of clinical performance and safety.

Key Responsibilities:

  • Maintain and enhance documentation related to clinical evaluations, post-market clinical follow-ups, and post-marketing surveillance.
  • Facilitate cross-departmental communication with teams such as Marketing and R&D to ensure that all necessary documentation is current and comprehensive.
  • Oversee external service providers to assist in the preparation of clinical evaluation documentation, PMCF, and PMS.
  • Establish clinical evidence requirements in compliance with MDR and relevant MDCGs.
  • Assess equivalence to existing devices when necessary, adhering to MDRs and applicable MDCGs.
  • Conduct searches in pertinent vigilance databases.
  • Provide support for risk analysis and study planning for CE and PMCF studies.

Qualifications:

  • A university degree in life sciences, natural sciences, or a related field.
  • Professional experience in the medical device sector or a similar regulatory environment.
  • In-depth knowledge of regulatory requirements, including MDR and relevant MDCGs.
  • Proficiency in literature search and review, along with expertise in regulatory medical writing.
  • Familiarity with database management systems.
  • A collaborative and professional approach when engaging with stakeholders.
  • Strong IT skills, particularly with the MS Office suite.
  • Fluency in written and spoken English.

Benefits:

  • Flexible working arrangements, including adaptable hours and remote work options.
  • International mobility opportunities.
  • Supportive policies for work-life balance, including childcare subsidies.
  • Generous paid leave, plus additional leave for significant life events, along with vacation pay and special annual bonuses as per collective agreements.
  • Company pension scheme with attractive employer contributions, including a matching model for deferred compensation.
  • Ample parking, on-site dining facilities, and various employee shop offerings.
  • Access to a wide range of fitness and wellness facilities, including over 6000 gyms and studios.
  • Comprehensive health and wellness programs, including skin cancer screenings and mental health courses.
  • Job bike leasing options.
  • Exclusive discounts on travel, fashion, and technology through our corporate benefits platform.

Shape a career that is dedicated to healthcare customers, prepared for future challenges, and rooted in a culture of trust and transparency.