Senior Quality Assurance Professional (Pharmaceutical, Hellerup)

Job summary

This role involves overseeing quality assurance processes for commercial drug products and finished goods within the pharmaceutical sector. The position is based in Hellerup, Denmark, and requires collaboration with both internal teams and external contract manufacturing organizations (CMOs).

Qualifications

• Master’s degree in natural science, preferably MSc. Pharm.
• 2-5 years of experience in the pharmaceutical industry.
• Knowledge of Good Manufacturing Practices (GMP).

Responsibilities

• Review batch documentation and quality records, including deviations and CAPAs.
• Collaborate with internal and external stakeholders, particularly CMOs.
• Support planning and oversight of departmental tasks, including product release.
• Assist with updates to standard operating procedures (SOPs) and annual product quality reviews (APQR).

Skills

• Strong analytical skills and a quality-focused mindset.
• Ability to work cooperatively with diverse stakeholders.
• Proficient in English, both written and spoken.
• Proficient in MS Office.

Education

• Master’s degree in natural science, preferably MSc. Pharm.

Tools

• MS Office