Facilities Deviation Writer
Novartis is hiring a Facilities Deviation Writer. Level rates it ; you can apply on Level.
AI in this role
Job Description Summary
#LI-HybridLocation: 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.
Job Description
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 in a pharmaceutical, facilities, engineering, or quality environment
Hands-on experience with deviation management and writing investigations in a GMP environment
Proven experience in CAPA management, including creation, implementation, and effectiveness tracking
Strong root cause analysis skills using structured investigation methodologies
Strong understanding of current good manufacturing practices and regulatory expectations for biologics manufacturing
Excellent technical writing skills, with the ability to clearly structure investigations and present findings
Commitment to Diversity and Inclusion
Novartis is committed to building an outstanding, inclusive work environment and diverse team representative of the patients and communities we serve.
Accessibility and accommodation
Novartis is committed to work with and provide reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to tas.mexico@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Skills Desired
Business Processes, Data Analytics, digital skills (Inactive), General Hse Knowledge (Inactive), Good Manufacturing Practices (GMP), ResilienceHow we rate this
Facilities Deviation Writer at Novartis rates 29 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Open the description and count.
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