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Location: Hillerød, Zealand Region
Category: Quality and Compliance
Salary: Apply for details
Country: Denmark
Employment: Contract
Worksite: On-Site
3 month contract · full time · on-site
A leading international biopharmaceutical manufacturing organisation is seeking an experienced Senior DPM Quality Assurance Associate to support operations within a sterile Drug Product Manufacturing environment.
Working closely with the Quality Assurance team, you will be responsible for the review and management of key quality records supporting manufacturing operations. This is a hands‑on QA role requiring strong GMP expertise, excellent stakeholder engagement skills and the ability to drive high quality documentation and compliance standards.