QA Associate – Complaint Management

About the role

Join Ascendis Pharma as a QA Associate focused on complaint management, supporting both marketed products and those in clinical development. You will work globally, collaborating with cross‑functional teams and CMOs from the Hellerup headquarters.

Key responsibilities

• Handle complaints in Veeva QMS, providing support, coordination and stakeholder communication.
• Drive quality improvement initiatives across the organization.

Required profile

• Natural Science degree with 2–5 years of experience in the life‑science healthcare industry.
• Experience working under GMP regulations.
• Proven ability to manage multiple tasks in a fast‑paced environment.

Required skills

• Complaint handling for pharmaceutical, medical device, or drug‑device combination products.
• Proficiency with Veeva QMS.
• Professional level written and spoken English.