Quality Specialist
Pubblicato il 12-08-2026 - Thermo Fisher Scientific in Monza
**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **pecific tasks/primary activities**: - Contribute to ensuring the pharmaceutical production of sterile injectables is flawless and adheres strictly to current US GMP and EU GMP regulations.
- Successfully implement improvement interventions and maintain world-class quality standards. **Control**: - Ensure constant and meticulous monitoring of production lines to maintain compliance with all regulatory and company standards. **Quality**: - Participate in defining and coordinating the testing and validation of machinery, ensuring strict adherence to GMP regulations.
- Conduct audits and complete any necessary corrective actions to maintain quality.
- Analyze defects and complaints, determining and implementing necessary actions for improvement.
- Propose and conduct GMP training courses to improve operational activities. **Procedures**:
**Client**: - Interact with clients to discuss changes and update procedures accordingly, encouraging collaborative relationships and ensuring client happiness.
**Requirements and qualifications**: - Bachelor’s Degree in a scientific/pharmaceutical area (FCT, Pharmacy, Chemistry, Biotechnology) or equivalent experience.
- Proven knowledge of machinery, systems, and methodologies for drug production.
- In-depth understanding of GMP regulations.
- Proficient in using main information systems. **Professional experiences**: - Proven experience in QA/Production within pharmaceutical companies. **Consolidated experience in QA/Production in pharmaceutical companies**: - Demonstrated expertise in QA/Production, with a proven track record in the pharmaceutical industry. **Languages**: - Proficiency in English required. **Personality traits**: - Shows a strong focus on organization and attention to detail.
- Strong observational skills.
- Outstanding relational and conflict management abilities.
- Critical thinking and ambitious approach.