Quality
Associate Director, GCP Quality
Resumé
The Associate Director, GCP Quality plans and performs GCP audits, supports regulatory inspections, and provides compliance advice and quality partnership across clinical development teams.
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Kort om jobbet
Are you passionate about driving GCP compliance and quality excellence across global clinical development programs? If so, now is your chance to join Ascendis Pharma as our new Associate Director, GCP Quality. Ascendis Pharma is a global biopharmaceutical company committed to making a meaningful difference in patients’ lives.
Guided by our core values of Patients, Science, and Passion, we are applying our innovative TransCon® technology platform to fulfill our mission of developing new therapies that demonstrate best-in-class potential to address unmet medical needs.
At our headquarters in Hellerup, Denmark, research facilities in Heidelberg, Germany, and additional offices across Europe and the United States, we are advancing programs in our Endocrinology Rare Disease and Oncology portfolios. We also collaborate with partners on the development of TransCon-based products in other therapeutic areas and markets.
We are seeking a passionate Associate Director, GCP Quality to join our growing team. As a key member of the Ascendis Pharma team, you will play a crucial role in performing GCP audits. This is an exciting opportunity to work in a fast-paced environment, collaborate with cross-functional, global teams working together to achieve extraordinary results1 …
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