Mes System Editing & Maintenance

Data di pubblicazione: 2026-11-10
Sedi dell'annuncio: Torre Annunziata
Sedi in Campania: Torre Annunziata (NA)

# MES System Editing & Maintenance

Azienda: Novartis

Sede di lavoro: Torre Annunziata

Tipo di impiego: Full time

**Salary Range:**

€31,300.00 - €58,100.00

**Job Description Summary**

#LI-Onsite

Location: Torre Annunziata, Italy

Relocation Support: This role is based in Torre Annunziata, Italy. Novartis is unable to offer relocation support: please only apply if accessible.

You’ll help shape the digital backbone of ophthalmic manufacturing, turning complex production requirements into reliable, compliant solutions that work where they matter most: on the shop floor. As MES System Editing & Maintenance, you’ll connect Manufacturing, Quality, Supply Chain, Engineering, Automation, Validation and IT/OT to strengthen electronic batch records, process orders and manufacturing master data across production and packaging. From new product introductions and system start-ups to day-to-day troubleshooting and continuous improvement, your expertise will help enable efficient execution, robust data integrity and inspection-ready operations while creating simpler, more reliable ways of working.

**Job Description**

Deadline for applications: **25th of November 2026.**

**Key Responsibilities:**

- Create, configure and maintain electronic Master Batch Records, recipes and digital workflows for ophthalmic manufacturing and packaging.
- Translate process, equipment and quality requirements into robust, executable Manufacturing Execution System workflows.
- Maintain process orders, production data and manufacturing master data to support timely, compliant production.
- Provide functional support and troubleshoot system, process-order, master-data and equipment-interface issues during manufacturing operations.
- Monitor integrations between Manufacturing Execution Systems, SAP, automation and Track & Trace systems, coordinating resolution of interface issues.
- Support deviations, corrective and preventive actions, change controls and validation activities while protecting the validated state.
- Enable new product introductions, qualification activities, system go-lives and production ramp-ups across ophthalmic manufacturing and packaging.
- Drive continuous improvement, training and knowledge sharing to strengthen system reliability, right-first-time execution and user experience.

**Essential Requirements**:

- Experience working with Manufacturing Execution Systems and electronic batch records in a regulated manufacturing environment.
- Strong understanding of manufacturing master data, process orders, recipes and electronic production workflows.
- Knowledge of Good Manufacturing Practice, data integrity, Good Documentation Practice and computerized system validation principles.
- Ability to troubleshoot manufacturing-system, master-data, process-order and system-interface issues using structured problem-solving approaches.
- Strong cross-functional collaboration skills, with the ability to translate manufacturing requirements into reliable digital solutions.
- Fluent Italian and professional working proficiency in English for technical documentation and international collaboration.

**Rewards**

At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.