Resumen
This role is essential in ensuring the smooth operation and continuous improvement of MES systems across all Novartis RLT sites, contributing significantly to the organization's efficiency and compliance standards.
About the Role
Role Responsibilities:
- Designing and updating MBRs in alignment with global core processes.
- Providing business support during Site MES Deployment Projects.
- Conducting site Process Analysis and fit-gap analysis for project preparation in coordination with Global Process Business Owners.
- Managing and updating guidelines based on global MES governance rules.
- Reviewing and consolidating MES software errors, prioritizing fixes in collaboration with the MES IT team.
- Attending Change Advisory Board meetings and prioritizing MES Business Change requests.
- Ensuring effective collaboration across all business units and manufacturing facilities.
- Maintaining the Global Process Model and conducting regular training sessions on MES.
Role Requirements:
- Experience in MBR design, preferably within the pharmaceutical industry.
- Proven track record of collaborating across boundaries and influencing without authority.
- Interaction with senior management and leveraging digital technology/big data.
- Relationship management experience and multinational global exposure.
- Fluency in Italian and English (written and spoken)
#LI-Onsite
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