Aktuelle Jobs im Zusammenhang mit Regulatory Compliance Expert - Penzberg, Bayern - GULP – experts united


  • Penzberg, Bayern, Deutschland Randstad Deutschland Vollzeit

    Compliance Specialist in PenzbergWe are looking for a Compliance Specialist to support our clinical trial supply management, drug-related distribution and storage. As a Compliance Specialist, you will be responsible for ensuring that all activities are in compliance with GxP regulations.Key Responsibilities:Support GxP compliance of all activities in the...

  • Submission Manager

    vor 2 Wochen


    Penzberg, Bayern, Deutschland Roche Vollzeit

    Job SummaryThe Submission Manager plays a crucial role in delivering high-quality regulatory submissions to Health Authorities worldwide. This position requires strong technical document editing skills, regulatory knowledge, and excellent communication abilities.Key ResponsibilitiesEdit complex technical documents for clarity, grammar, spelling, and...


  • Penzberg, Bayern, Deutschland Roche Vollzeit

    Job SummaryThe Regulatory Submission Manager is responsible for delivering high-quality regulatory submissions to Health Authorities worldwide. This role involves editing complex technical documents, managing submission projects, and applying submission management skills to contribute to the daily business of Pharma Technical Regulatory submissions.Key...


  • Penzberg, Bayern, Deutschland GULP – experts united Vollzeit

    Are you a detail-oriented professional with a passion for ensuring the highest standards of quality and compliance in IT operations? We're looking for a Senior IT Compliance Specialist to join our team at GULP – experts united.As a key member of our IT compliance team, you will be responsible for ensuring that our IT systems and processes meet the highest...


  • Penzberg, Bayern, Deutschland GULP – experts united Vollzeit

    Join Our Team as an ITOT Compliance ExpertWe are seeking a highly skilled ITOT Compliance expert to join our dynamic team at GULP – experts united. As an ITOT Compliance expert, you will play a crucial role in ensuring the quality and compliance of our medical solutions.About the RoleAs an ITOT Compliance expert, you will be responsible for creating,...


  • Penzberg, Bayern, Deutschland GULP – experts united Vollzeit

    Join Our Team as an ITOT Compliance ExpertWe are seeking a highly skilled ITOT Compliance expert to join our dynamic team at GULP – experts united. As an ITOT Compliance expert, you will play a crucial role in ensuring the quality and compliance of our medical solutions.About the RoleAs an ITOT Compliance expert, you will be responsible for creating,...


  • Penzberg, Bayern, Deutschland GULP – experts united Vollzeit

    We are seeking a highly skilled Quality Assurance Manager to join our team at GULP – experts united. As a key member of our quality team, you will play a crucial role in ensuring the highest standards of quality in our pharmaceutical manufacturing processes.About the RoleSupport the development and implementation of quality management systems and processes...


  • Penzberg, Bayern, Deutschland GULP – experts united Vollzeit

    We are seeking a highly skilled Quality Assurance Manager to join our team at GULP – experts united. As a key member of our quality team, you will play a crucial role in ensuring the highest standards of quality in our pharmaceutical manufacturing processes.About the RoleSupport the development and implementation of quality management systems and processes...

  • Submission Manager

    vor 3 Wochen


    Penzberg, Bayern, Deutschland Roche Vollzeit

    Job SummaryThe Regulatory Submission Manager at Roche is responsible for delivering high-quality regulatory submissions to Health Authorities worldwide. This role involves editing complex technical documents, managing the flow of information, and ensuring data accuracy and quality.Key ResponsibilitiesEdit complex technical documents for clarity, grammar,...


  • Penzberg, Bayern, Deutschland GULP – experts united Vollzeit

    At GULP – experts united, we are seeking a highly skilled ITOT Compliance Specialist to join our dynamic team in Penzberg. As an ITOT Compliance Specialist, you will play a crucial role in ensuring the quality and compliance of our IT and automation systems.Key Responsibilities:Creation, processing, follow-up, and closure of changes, deviations,...

  • Biotechnology Expert

    vor 3 Wochen


    Penzberg, Bayern, Deutschland GULP – experts united Vollzeit

    Are you a skilled professional looking for a new challenge in the field of pharmaceutical compliance? GULP – experts united has an exciting opportunity for a Biotechnology Expert to join our team.Key Responsibilities:Creation, processing, and closure of changes, deviations, corrections, and preventive measuresPerforming quality assurance tasks for QA, IT,...


  • Penzberg, Bayern, Deutschland GULP – experts united Vollzeit

    We are seeking a highly skilled Quality Assurance Manager to join our team at GULP – experts united. As a key member of our quality team, you will be responsible for ensuring the highest standards of quality in our pharmaceutical manufacturing processes.About the RoleSupport the development and implementation of quality management systems and...


  • Penzberg, Bayern, Deutschland GULP – experts united Vollzeit

    We are seeking a highly skilled Quality Assurance Manager to join our team at GULP – experts united. As a key member of our quality team, you will be responsible for ensuring the highest standards of quality in our pharmaceutical manufacturing processes.About the RoleSupport the development and implementation of quality management systems and...

  • Submission Manager

    vor 4 Wochen


    Penzberg, Bayern, Deutschland Roche Vollzeit

    About the RoleThe Submission Manager is a key member of our Regulatory Affairs team, responsible for delivering high-quality regulatory submissions to Health Authorities worldwide. This role requires strong editing skills, attention to detail, and the ability to work with complex technical documents.Key ResponsibilitiesEdit complex technical documents for...

  • Submission Manager

    vor 4 Wochen


    Penzberg, Bayern, Deutschland Roche Vollzeit

    About the RoleThe Submission Manager is a key member of our Regulatory Affairs team, responsible for delivering high-quality regulatory submissions to Health Authorities worldwide. This role requires strong editing skills, attention to detail, and the ability to work with complex technical documents.Key ResponsibilitiesEdit complex technical documents for...


  • Penzberg, Bayern, Deutschland GULP – experts united Vollzeit

    As a key member of our team at GULP – experts united, you will play a vital role in ensuring the highest standards of quality and compliance in our medical solutions.Our team in Penzberg is dedicated to pioneering research and development, and we are seeking a highly skilled ITOT Compliance employee to join our dynamic team.Key responsibilities...

  • Submission Manager

    vor 3 Wochen


    Penzberg, Bayern, Deutschland Roche Vollzeit

    About the RoleThe Submission Manager plays a critical role in delivering high-quality regulatory submissions to Health Authorities worldwide. This position requires strong editing skills, attention to detail, and the ability to manage complex technical documents.Key ResponsibilitiesEdit complex technical documents for clarity, grammar, spelling, and...

  • Submission Manager

    vor 3 Wochen


    Penzberg, Bayern, Deutschland Roche Vollzeit

    About the RoleThe Submission Manager plays a critical role in delivering high-quality regulatory submissions to Health Authorities worldwide. This position requires strong editing skills, attention to detail, and the ability to manage complex technical documents.Key ResponsibilitiesEdit complex technical documents for clarity, grammar, spelling, and...


  • Penzberg, Bayern, Deutschland GULP – experts united Vollzeit

    Are you a detail-oriented professional with a passion for quality and compliance? Do you have experience in the pharmaceutical industry and a strong understanding of regulatory requirements? We are currently looking for an Employee Quality & Compliance Specialist to join our team at GULP – experts united.Key Responsibilities:Support the Group Manager and...


  • Penzberg, Bayern, Deutschland GULP – experts united Vollzeit

    Are you a detail-oriented professional with a passion for quality and compliance? Do you have experience in the pharmaceutical industry and a strong understanding of regulatory requirements? We are currently looking for an Employee Quality & Compliance Specialist to join our team at GULP – experts united.Key Responsibilities:Support the Group Manager and...

Regulatory Compliance Expert

vor 2 Monaten


Penzberg, Bayern, Deutschland GULP – experts united Vollzeit

Are you a detail-oriented professional looking for a new challenge in the pharmaceutical industry?

We are seeking a Compliance Specialist to join our team at GULP – experts united. As a Compliance Specialist, you will play a critical role in ensuring the quality and integrity of our clinical trial supply management, drug-related distribution, and storage processes.

Key Responsibilities:

  • Support the development and implementation of GxP compliance strategies and procedures
  • Ensure compliance with regulatory requirements and industry standards
  • Collaborate with cross-functional teams to identify and mitigate compliance risks
  • Develop and maintain GxP documentation and training programs
  • Conduct audits and inspections to ensure compliance with GxP regulations

Requirements:

  • University degree in a scientific field or a related discipline
  • Several years of experience in the pharmaceutical or biotech industry
  • Knowledge of quality standards (GMP, GCP, GDP) and regulatory requirements
  • Strong analytical and problem-solving skills
  • Excellent communication and interpersonal skills

What We Offer:

  • A dynamic and collaborative work environment
  • Opportunities for professional growth and development
  • A competitive salary and benefits package

We welcome applications from qualified professionals who are passionate about ensuring the highest standards of quality and compliance in the pharmaceutical industry.