Quality Management Specialist (m/f/d)

Allogenetics GmbH; Hannover; Hybrid; Vertraulich; Vollzeit

Zusammenfassung

A rapidly growing biotech start-up based in Hannover is looking for a Quality Management Specialist (m/f/d). In this role, you will ensure the implementation and continuous improvement of a GxP-compliant Quality Management System. You will support clinical development activities, manage quality risks, and collaborate with cross-functional teams. If you have experience in Quality Management Systems and a strong background in life sciences, we look forward to receiving your application.

Leistungen

Competitive compensation

Flexible working hours

Professional development opportunities

Qualifikationen

• Experience with Quality Management Systems (QMS) in complex environments.
• Knowledge of quality standards and regulatory requirements (ICH GCP, EU GMP).
• High sense of responsibility and reliability.

Aufgaben

• Implement and improve a GxP-compliant Quality Management System.
• Support clinical development activities and manage quality risks.
• Conduct audits and inspections for compliance.

Kenntnisse

Attention to detail

Project management skills

Problem-solving abilities

Teamwork abilities

Excellent communication in English and German

Ausbildung

Degree in life sciences or related field

Jobbeschreibung

Overview

Allogenetics GmbH is a spin-off of the Hannover Medical School and a rapidly growing biotech start-up based in Hannover. Together, we are shaping the future of transplantation medicine by developing therapies that prevent organ rejection after transplantation. This work has a meaningful impact on patients worldwide.

As part of our team, you will work on a project that combines medical innovation with significant societal impact. We operate in a dynamic environment characterised by flat hierarchies, interdisciplinary collaboration and an open, appreciative culture.

To support our team, we are looking for a Quality Management Specialist (m/f/d) to join us as soon as possible.

Tasks

🔬 Your Key Tasks

You ensure the implementation and continuous improvement of a GxP-compliant Quality Management System and maintain compliance with Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP) standards. In this role, you support clinical development activities, manage quality risks and CAPAs, and collaborate closely with cross-functional teams.

• Develop and implement a Quality Management System (QMS) aligned with GxP standards, ensuring compliance with Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP) throughout product and clinical development.
• Define quality objectives and establish a strategic quality program, including organizational policies and procedures.
• Develop and maintain comprehensive quality documentation, such as manuals, SOPs, and protocols.
• Identifying and assess quality risks, implementing effective mitigation strategies through robust risk management practices.
• Address quality issues, monitor and review corrective actions (deviation and CAPA management).
• Continuously improve processes to enhance product and service quality.
• Support sponsor responsibilities in clinical trials, ensuring adherence to regulatory and ethical standards.
• Plan and conduct internal and external audits and inspections to verify compliance with applicable regulations and guidelines.
• Provide training and support to staff on quality-related topics, fostering a culture of quality and compliance.
• Serve as the primary contact point for quality and compliance inquiries, offering expert advice and solutions.

Requirements

🧪 Your Profile

• Degree in life sciences or related field (or equivalent professional experience)
• Experience with Quality Management Systems (QMS) and process development in complex environments (e.g., clinical trials)
• Knowledge of quality standards and regulatory requirements (e.g., ICH GCP, EU GMP)
• Strong attention to detail, organizational, and project management skills
• Effective problem-solving and teamwork abilities
• Excellent communication skills in English and German
• High sense of responsibility and reliability

Benefits

💡 What we offer:

• A meaningful role that contributes directly to innovations in transplantation medicine.
• Competitive compensation and flexible working hours, including the option to work partially remotely.
• Hands-on experience in a dynamic biotech environment, where you can contribute ideas and take ownership of your work.
• Varied and challenging tasks with room for professional creativity and initiative.
• An international perspective in a cutting-edge field of medical innovation.
• Long-term development opportunities and career growth within the company.

👉 Transparency matters to us.

As a young biotech start-up, we are gradually expanding our benefits package, particularly with regard to professional development and work-life balance.

🤝 Equal opportunities

Allogenetics is committed to diversity and equal opportunities. We expressly encourage applications from women. Candidates with disabilities will be given preferential consideration if equally qualified.

🌟 Make your talent count where it really matters!

At Allogenetics, we are working to improve the lives of transplant patients by delivering genuine medical innovation with meaningful societal impact. If you want to contribute and help shape the future, we look forward to receiving your application. Together, we create solutions that save lives and redefine the future of medicine.

Interested?

We look forward to receiving your application here or via email at [e-mail]. We are hiring as soon as possible and have designed our application process to be quick and simple, so you will receive feedback promptly.