Quality Management Specialist (m/f/d) für Hannover gesucht
Arbeits- und Stellenangebot im Regiobizz Arbeitsmarkt
Job Kategorie: Medizin/Pharma/Biotech Medizin/Pharma/Pflege
Stellenangebot Basisdaten
- Arbeitsort:
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DE 30625 Hannover
- Umkreis:
-
keine Angabe.
- Art der Arbeitsstelle:
-
- Letze Aktualisierung:
-
05.03.20262026-03-05
Stellenausschreibung: Quality Management Specialist (m/f/d)
- Arbeitgeber bzw.
Arbeitsvermittler
-
Allogenetics GmbH in Hamburg
- Branche
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Medizin/Pharma/Biotech
- Kategorie
-
Medizin/Pharma/Pflege
- Stellenbeschreibung
- 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 hr@allogenetics.com. We are hiring as soon as possible and
have designed our application process to be quick and simple, so you
will receive feedback promptly.
- Qualifikation
- Arbeitskräfte
- Verdienst:
- n.a.
- Bewerbung an
- Allogenetics GmbH
Am Strandkai 1
De 20457 Hamburg
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