Key skills
CommunicationCritical ThinkingTime Management
About this role
Role Overview
- Manage deviations, OOS, and reprocessing/rework, ensuring their analysis, documentation, and closure in accordance with GMP.
- Administer and keeping the risk analysis system and the full CAPA cycle up to date.
- Investigate quality complaints and coordinating actions with the involved areas until resolution.
- Participate in internal audits and inspections, driving the fulfillment of corrective and preventive actions.
- Contribute to Quality Committees through the presentation of KPIs and relevant findings.
- Providing GMP training and onboarding to personnel to strengthen the quality culture within the plant.
Requirements
- Degree in Pharmaceutical Chemistry, Chemistry, Chemical Engineering, or related fields.
- More than three years of experience in activities related to production or quality within the Pharmaceutical Industry or similar sectors.
- Strong analytical skills, critical thinking, and a focus on continuous improvement.
- Solid communication skills with the ability to influence, persuade, and build alignment with operational, technical areas, and suppliers.
- Strong knowledge of GMP and quality systems.
- Organization, time management, and strong attention to documentation accuracy.
Benefits
- Health insurance
- Professional development opportunities