16 ott - Monza
Experteer Italy
As Lead QA Technician, you ensure product quality and regulatory compliance within pharmaceutical manufacturing. You will work as part of the Quality team to uphold high standards and support life-changing medicines. Expect to investigate deviations, manage CAPA, and help prepare for regulatory inspections in an aseptic environment. You will collaborate with cross-functional teams to maintain compliant documentation and processes, contributing to the mission of making the world healthier, cleaner and safer. This role offers the chance to shape quality programs in a global, fast-paced setting.
La preghiamo di verificare di possedere il livello di esperienza e le qualifiche adeguate leggendo la panoramica completa di questa possibilità qui sotto.
- Quality oversight of pharmaceutical manufacturing operations
- Batch record review and deviation investigations
- CAPA management and effectiveness verification
- Support regulatory inspections and customer audits
- Maintain and improve quality systems and documentation (TrackWise, Documentum)
- Collaborate with cross-functional teams to address quality issues
- Ensure aseptic manufacturing processes and clean room controls
- Communicate findings clearly and drive corrective actions
- Guide and develop team members on quality practices
- Manage multiple priorities in a dynamic environment
- 4 years of experience in pharmaceutical quality assurance or related GMP environment
- Comprehensive knowledge of GMP regulations, FDA guidelines and quality systems
- Experience with batch record review, deviation investigations and CAPA management
- Strong understanding of aseptic manufacturing processes and controls
- Advanced proficiency in quality documentation systems (e.g. TrackWise, Documentum)
- Professional communication skills (written and spoken)
- Ability to manage multiple priorities and work under pressure
- Strong attention to detail and analytical problem-solving skills
- Interpersonal and xysqume communication abilitie
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