**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.