Passionate about Quality Assurance with expertise within outsourced GMP activities and development projects?
Ascendis Pharma invites you to explore the role of our newest QA Specialist / QA Professional for Development GMP activities.
With roots spanning Denmark, Germany, and the United States, Ascendis Pharma A/S emerges as an innovative and dynamic biopharmaceutical Company. Powered by our innovative TransCon technology, we're creating a fully integrated biopharmaceutical enterprise dedicated to transforming the life of patients. Guided by our core principles of patients, science, and passion, we leverage our TransCon drug development platform to pioneer new therapies addressing critical medical needs. Our pipeline consists of several therapies, each designed to set new standards in patient care.
We're on the lookout for a dedicated QA Specialist, or Professional - depending on qualifications, to join our highly skilled QA team in Copenhagen. As a vital contributor at Ascendis Pharma, you'll play a pivotal role in ensuring the QA oversight of the outsourced development activities carried out at our Contract Laboratories and Manufacturing Organizations. Working in a dynamic environment alongside global teams to achieve our final goals to deliver best in class products to our Clinical programs’ remarkable outcomes.
You'll become part of the Development QA - Chemistry team, working closely with 10 colleagues and reporting to Director Jon Wriedt Poulsen, based in Hellerup, Copenhagen, Denmark, where your home base will also be.
Your main responsibilities will include:
Qualifications and Skills:
Key Competencies:
Travel: proximately 20 days per year.
Office: Tuborg Boulevard 12, 2900 Hellerup, Copenhagen Denmark
For more details about the job or the company, please contact: Jon Wriedt Poulsen, Director of QA Development Chemistry, [email protected]. All applications must be submitted in English and are treated confidentially.
Applications will be reviewed as they are received, so please apply promptly.
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