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Join us

InnoMedica's team lives creative thinking and innovation combined with professional competence and patient proximity. Are you motivated to become part of the young and dynamic team and committed to InnoMedica's goal of giving patients access to a new generation of nanomedicines? Apply now and make an active contribution to the company's success. We look forward to getting to know you.

Operational Manager Quality Assurance

As part of the Quality Assurance (QA) team, you will be responsible for maintaining and expanding the pharmaceutical quality system. The focus is on compliance with GMP guidelines, which ensure the quality of the manufactured products.

Your responsibilities include:

  • Management of GMP documentation and ensuring compliance with national and international standards
  • Responsibility for a small team
  • Responsibility for the internal audit and inspections by authorities
  • Responsibility for preparing batch documentation for certification by the responsible person for clinical trials
  • Participating in core quality assurance tasks, for example writing and reviewing deviation, CAPAs, change requests, SOPs, qualifications, and validations
  • Active involvement in interdepartmental projects teams (process engineering, production, quality control)
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Manager Clinical Research

As a part of the Clinical Research team,
the main objective of your work is the clinical development of InnoMedica's products with the aim of applying innovative drugs in clinical trials to patients and ultimately bringing them to market.

Your responsibilities include:

  • Responsibility for a team of seven
  • Overseeing and managing the department activities
  • Develop, implement and monitor the clinical research strategy
  • Ensure compliance with regulatory standards
  • Keeping track of resources, budget and timelines
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Scientist Quality Assurance

As part of the Quality Assurance (QA) team, you will be responsible for maintaining and expanding the pharmaceutical quality system. The focus is on compliance with GMP guidelines, which ensure the quality of the manufactured products.

Your responsibilities include:

  • Management of deviations, change requests as well as corrective actions and preventive actions
  • Review of equipment qualifications, batch documentations, and product release preparations for clinical studies
  • Project planning and coordination and active participation in interdisciplinary project teams
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Have you not found a suitable position for you and would still like to apply to us? Then send us your spontaneous application via hr@innomedica.com.