QA Associate - Patient Safety & Complaints

Ascendis Pharma; Hellerup; On-site; DKK 550,000 - 750,000; Full time

Job summary

Ascendis Pharma in Hellerup, Denmark, is seeking a QA Associate/QA Professional to join the Complaint Management Department. You will handle complaint processes for marketed products and products in Clinical Development, coordinating with global teams and CMOs.

The role requires a background in Natural Science with 2–5 years in life science, experience with GMP, and proficiency in English. You will report to Karina Bergenholtz, Director QA.

Qualifications

• Educational background in Natural Science with 2–5 years life science experience.
• Experience with GMP regulations.
• Experience with complaint handling for pharmaceutical products or medical devices.

Responsibilities

• Handle complaints in Veeva QMS, including support and coordination with stakeholders.
• Drive quality improvement initiatives across the organization.

Skills

Complaint handling

GMP regulations

English professional level

Education

Natural Science degree

Tools

Veeva QMS

Job description

Ascendis Pharma in Hellerup, Denmark, is seeking a QA Associate/QA Professional to join the Complaint Management Department. You will handle complaint processes for marketed products and products in Clinical Development, coordinating with global teams and CMOs.

The role requires a background in Natural Science with 2–5 years in life science, experience with GMP, and proficiency in English. You will report to Karina Bergenholtz, Director QA.