- Own and develop CMC (Module 3) content based on real technical knowledge.
- Contribute to formulation, manufacturing and control strategy decisions.
- Support lifecycle and post‑approval activities.
- Evaluate product quality and process performance.
- Solve real product and process challenges with scientific judgement.
Skills:
- 5–8 years of hands‑on experience in CMC (Drug Product) – essential.
- Strong background in formulation, manufacturing and quality.
- Solid understanding of cGMP and ICH (Q8, Q9, Q10).
- Ability to think critically and take technical decisions.
We are looking for true CMC profiles:
- You understand the product and the process.
- You contribute through technical expertise (Module 3).
This is not a Regulatory Affairs role.
Not suitable for Module 1, publishing or coordination‑focused profiles.
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📌 Cmc Senior Technician (Alcobendas)
🏢 Italfarmaco España
📍 Alcobendas
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