We are looking for a motivated and curious CAPA & Nonconformance Specialist to support quality investigations and improvements within a regulated medical device environment.This temporary position (until 31-Dec-2026) offers a unique opportunity to gain hands-on experience in quality systems, investigations, and cross-functional collaboration within the pharmaceutical/medical device industry.
You will work in an international and dynamic environment where communication, ownership, and collaboration are key.
Key Responsibilities
- Support and coordinate investigations of product and process nonconformances using structured root cause analysis tools (e.g., 5 Whys, Fishbone, basic Fault Tree Analysis)
- Drive and track CAPA and NC records from initiation to closure, ensuring clear documentation and timely follow-up
- Support the team in improving documentation, SOPs and quality processes
- Collaborate closely with Manufacturing, Quality, Supply Chain and other stakeholders to implement effective and sustainable solutions
- Assist in monitoring Key Performance Indicator (KPI) trends and identify recurring issues or improvement opportunities
- Contribute to audit readiness by supporting responses to audit observations and quality actions