**Overview** **Key Responsibilities**
- Draft, implement, and maintain the **GMP Manual**.
- Ensure that production processes comply with GMP requirements through regular **internal audits**.
- Conduct **GMP training sessions** for staff.
- Manage quality-related issues, identifying root causes and implementing **corrective and preventive actions (CAPA)**.
- Oversee equipment and instrument **maintenance activities**, ensuring proper documentation and follow-up.
- Prepare and maintain detailed **quality assurance reports and records**. **Requirements**: - Degree in Chemistry, Biology, Pharmacy, Engineering, or a related scientific field.
- Previous experience in Quality Assurance within a **GMP-regulated environment** (pharmaceutical, cosmetics, or related industries preferred).
- Strong knowledge of GMP standards and quality systems.
- Fluent in **English** (written and spoken).
- Excellent organizational, communication, and problem-solving skills.
- Ability to deliver effective training and work cross-functionally with different teams.
- Proficiency in **MS Office** and quality management tools. Contratto di lavoro: Tempo pieno, Tempo indeterminato Agevolazioni: - Buoni pasto
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