Facilities Deviation Writer (Ciudad de México)

Facilities Deviation Writer (Ciudad de México)

16 oct
|
MX06 (FCRS = MX006) Novartis Farmacéutica S.A. de
|
Ciudad de México

16 oct

MX06 (FCRS = MX006) Novartis Farmacéutica S.A. de

Ciudad de México

Job Description Summary#LI-Hybrid Location: Mexico City, Mexico Relocation Support: This role is based in Mexico City, Mexico. Novartis is unable to offer relocation support: please only apply if accessible. Take ownership of quality where it truly matters - at the intersection of facilities, engineering, and patient impact. In this role, you will play a key part in ensuring deviations are thoroughly investigated, understood, and resolved, helping to maintain high standards in a complex GMP environment. You’ll work closely with cross-functional teams to drive robust investigations and meaningful corrective actions, while shaping a culture of continuous improvement and quality excellence. If you enjoy combining analytical thinking with hands-on collaboration, this role offers a chance to make a real difference.
Key Responsibilities
- Open and assess deviations within required timelines, ensuring accurate classification and documentation
- Evaluate product impact of deviations, aligning with batch release requirements and quality standards
- Author, own,



and drive investigations through to timely and compliant closure; update SOPs as relevant to Deviations/CAPAs
- Apply structured root cause analysis methods to identify causes of process and product deviations
- Ensure investigations are complete, accurate, and fully supported with robust documentation
- Design and execute experiments or studies to support investigation outcomes
- Collaborate cross-functionally to assess deviation impact and maintain compliant operations
- Develop, document, and implement effective corrective and preventive actions
- Monitor CAPA effectiveness and ensure execution through Good Manufacturing Practice systems and training
- Deliver training and communication to reinforce quality practices and maintain compliance

Essential Requirements
- Bachelor’s degree in a relevant field with pharmaceutical industry experience
- Fluency in written and spoken English
- Two to five years of experience

📌 Facilities Deviation Writer (Ciudad de México)
🏢 MX06 (FCRS = MX006) Novartis Farmacéutica S.A. de
📍 Ciudad de México

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