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Clinical Practice QA Manager
We are looking for a new Good Clinical Practice QA Manager, who will be responsible for performing quality assurance activities to ensure that Calliditas’ clinical activities are conducted in accordance with Good Clinical Practice (GCP) guidelines, applicable regulations and Calliditas policies and procedures. The GCP QA Manager will report to the VP QA GxP and work in close collaboration with Clinical Operations, giving support and guidance within GCP. They will also be responsible for accurately identifying and communicating compliance risks and overseeing action plans to mitigate risks.
If you are interested, you can learn more about the position by following this link: https://www.linkedin.com/jobs/view/1933117721/
Head of Pharmaceutical Development & Manufacturing
We are looking for a talented individual to join us. The ideal candidate will manage a small internal team and a network of external consultants and suppliers to develop innovative formulations, optimize processes, oversee scale-up activities, manufacture clinical trial materials, write regulatory documents, and contribute to the overall pharmaceutical development activities. This person will provide knowledge-based leadership, coordination and management for multiple projects to successfully expedite product development and regulatory approvals and help satisfying unmet medical needs. If you are interested contact Rolf Carlsson or Martin Svensson through the below link.
Product Development Manager
Join us and make a difference! As PDM you will be responsible for providing expertise knowledge in the field of pharmaceutical development and process technology in projects. You will plan, design and oversee the implementation and progress at CDMOs, as well as ensuring appropriate documentation. If you are interested, you can read more and contact us through the below link.