Aktuelle Jobs im Zusammenhang mit Regulatory Compliance Specialist - Stuttgart, Baden-Württemberg - Catalyst Life Sciences


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  • Compliance Specialist

    vor 3 Wochen


    Stuttgart, Baden-Württemberg, Deutschland Piper Maddox Vollzeit

    Collaborate with Certification AuthoritiesWe are seeking a Compliance Specialist to collaborate with certification authorities and ensure compliance with industry standards (ARP 4754A).Key Responsibilities:Collaborate with certification authorities to ensure compliance with industry standardsDevelop and implement compliance strategies to meet regulatory...

  • Compliance Specialist

    vor 3 Wochen


    Stuttgart, Baden-Württemberg, Deutschland Piper Maddox Vollzeit

    Collaborate with Certification AuthoritiesWe are seeking a Compliance Specialist to collaborate with certification authorities and ensure compliance with industry standards (ARP 4754A).Key Responsibilities:Collaborate with certification authorities to ensure compliance with industry standardsDevelop and implement compliance strategies to meet regulatory...


  • Stuttgart, Baden-Württemberg, Deutschland SciPro Vollzeit

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  • Stuttgart, Baden-Württemberg, Deutschland Lapp Group Vollzeit

    Job DescriptionWe are seeking a highly skilled Product Compliance Specialist to join our team at Lapp Group. As a key member of our regulatory affairs team, you will be responsible for ensuring that our products comply with all relevant regulations and standards.Key ResponsibilitiesMonitor and analyze regulatory requirements for our productsIdentify and...

Regulatory Compliance Specialist

vor 2 Monaten


Stuttgart, Baden-Württemberg, Deutschland Catalyst Life Sciences Vollzeit
Compliance Engineer

Catalyst Life Sciences is seeking a highly skilled Compliance Engineer to join our team. As a Compliance Engineer, you will play a critical role in ensuring our medical devices meet the highest regulatory standards.

Key Responsibilities:
  • Develop and implement design control processes for development projects
  • Manage and maintain technical documentation
  • Collaborate with regulatory, quality assurance, project, and product management teams
  • Plan and support verification and validation activities
  • Contribute to risk management and audits
Requirements:
  • Relevant degree in medical technology or a related field
  • Knowledge of MDR, FDA, and ISO standards
  • Proficiency in English (C1) and German

Catalyst Life Sciences is committed to creating an inclusive and diverse work environment. We welcome applications from qualified candidates who share our values and are passionate about delivering high-quality medical devices.