QA Associate, Complaint Management
- Level
- Mid
Not stated in the posting: salary, work type, visa.
Open. First seen 30 October 2026.
About the role
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/Professional.
Ascendis Pharma's standard text
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 QA Associate/QA Professional to join our growing 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 Department consisting of 8 colleagues, and report directly to Karina Bergenholtz, Director QAwho is based in Hellerup. You will be based in Hellerup.
Your key responsibilities will be:
- Complaint handling in Veeva QMS, incl. support, coordination and contact to stakeholders
- Drive quality improvement initiatives across the organization
Qualifications and Skills:
You have an educational background in Natural Science with minimum 2-5 years’ experience within the life science healthcare industry. Additionally, we expect that you have experience working with GMP regulations.
Furthermore, you have:
- Experience with complaint handling for pharmaceutical products, medical devices and/or drug-device combination products
- The ability to manage multiple tasks and priorities in a dynamic, fast-paced environment
- A structured and quality-focused approach to operational tasks
- Proficiency in written and spoken English at a professional level
Key competencies:
You are a strong team player, analytical, and have a can-do attitude.
Ascendis Pharma's standard text
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 also expect you to 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.
Travel: 0 days per year.
Office: Tuborg Boulevard 12, 2900 Hellerup
Ascendis Pharma's standard text
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 Karina Bergenholtz, Director QA, 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.
Ascendis Pharma's standard text
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.
What this role asks for
60% of this description is written for the role. The rest is Ascendis Pharma's standard text, folded away below.
Compared with Ascendis Pharma's other open jobs.
The team: Product Supply & Quality
This role is one of 4 open in Product Supply & Quality. 3 were posted in the last 30 days.
WHAT THE TEAM WORKS WITH, ACROSS ITS POSTINGS
Power BI (1 of 4)
OTHER ROLES ON THIS TEAM
- (Senior) Project Manager/Process Specialist, Drug Substance Manufacturing posted Oct 19
- Senior QA Medical Device Specialist posted Oct 8
- Student Assistant - Master Data & Digital Solutions posted Sep 28
From the team and dates on Ascendis Pharma's own job board.
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