QA Associate - Complaint Management job opportunity at Ascendis Pharma.



Date2026-02-24T15:20:45.512Z bot
Ascendis Pharma QA Associate - Complaint Management
Experience: 5-years
Pattern: Full-time
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degreeAssociate
loacation Hellerup, Denmark
loacation Hellerup....Denmark

Are you passionate about Patient Safety? Do you have experience within Complaint Handling? If so, now is your chance to join Ascendis Pharma as our new QA Associate – Complaint Management. 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. From 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. Furthermore, we collaborate with partners on the development of TransCon-based products in other therapeutic areas and markets. We are seeking  a passionate QA Associate to join our team. As a key member of the Ascendis Pharma team, you will play a crucial role in complaint management and handle complaint processes regarding both marketed products as well as products in Clinical Development. You will work globally and have wide collaboration across the organization and towards CMOs. This is an exciting opportunity to work in a fast-paced environment, collaborate with cross-functional, global teams working together to achieve extraordinary results. You will be joining the Complaint Management team consisting of 8 colleagues, and report directly to Karina Bergenholtz, Director QA, who is based in Hellerup. You will be based in Hellerup. Your key responsibilities will be: Complaint management, incl. support, coordination and contact to stakeholders Qualifications and Skills: You have an educational background in Natural Science with minimum 2-5 years’ experience within the life science industry. Additionally, we expect that you have experience working with GMP regulations. Furthermore, you are: Experienced with complaint processing of either drugs, medical devices and/or drug-device combination products. Able to thrive in a dynamic environment and enjoys taking on a variety of operational tasks. Proficient in English at a professional level, both written and spoken. Key competencies: You are a strong team player, analytical, and have a can-do attitude. You possess an entrepreneurial mindset and can thrive in an informal, open environment where innovation and change are key.   To succeed in this role, we believe that you should be self-driven and like to work in a collaborative environment. Moreover, you are pragmatic with an open and communicative approach and is thus inspired to find new and smart ways to fulfil quality requirements. Office:  Tuborg Boulevard 12, 2900 Hellerup  Apply now. We evaluate applications when received, so we encourage you to apply as soon as possible. Please note that we conduct interviews on a rolling basis and reserve the right to remove the job posting at any time.    To ensure your application is reviewed, please submit it through the specified platform - applications sent by email or other channels will not be evaluated.  For more details about the position or the company, please contact Director of Complaint Management, Karina Bergenholtz, kab@ascendispharma.com You can learn more about Ascendis by visiting our website www.ascendispharma.com Applications must be submitted in English and will be treated confidentially.   A note to recruiters: We do not allow external search party solicitation.  Presentation of candidates without written permission from the Ascendis Pharma HR team (specifically from: Talent Acquisition Partner or Human Resources Director) is not allowed.  If this occurs, your ownership of these candidates will not be acknowledged.

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