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Sr Manager Process Analytics & Automation

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Job Id JOB ID-13442 Standort Toulouse, Frankreich Veröffentlichungsdatum 01/19/2026 Job Kategorie Enabling Functions

Job Title: Process Analytics and Automation Manager

Type of contract - CDI

Location: Toulouse
Department: MSAT
Reports To: MSAT Director

We’re excited to share this opportunity is part of the Sandoz acquisition of Just-Evotec Biologics in Toulouse. Through this opportunity you will impact the lives of hundreds of millions of people through bold ideas supported by an inclusive, agile company culture. Join us to help make healthcare fairer and faster, help us to pioneer access to medicine! Click to learn more.

What You’ll Do:

  • Manage the team of both Automation team and Process Data analytics team to Support Manufacturing operations

  • Strives to Develop and Implement a data driven process control mindset with highly reliable automated systems and strong data analytics template.

  • Collaborate with IT to create and maintain a robust IT-OT interface and enhance data management/engineering

  • Strongly interact with all stakeholders (Manufacturing, Process, Quality…) to develop solutions adapted to their needs with a “self-service” data analytics target.  

  • Support and collaborate in Digital roadmap definition and deployment.

  • Ensure automated systems and data template are and remain GMP compliant from the source to end-user and along their full-life cycle.

  • In charge of maintaining automated system continuously running in production within a GMP environment

  • Lead implementation of new Automated technologies in production.

  • Support CSV activities bringing expertise and leadership

Who You Are:

  • Bachelor’s degree in Process Engineering, Automation Engineering or related program with 8+ years relevant experience.

  • At least 5+ years of Experience in managing technical teams in bio-pharma industry (GxP environment).

  • At least 3+ years of Experience deploying data analytics in industry and deployment of Data management platform within a GMP environement

  • Experience with System commissioning, qualification, and validation activities and data template validation

  • High level of knowledge in data analytics and associated programming methods

  • Good knowledge in statistical methods to analyze process data

  • Familiar with troubleshooting approach and methodologies (i.e. RCA , DMAIC…)

  • Authoring technical and quality documentation within GMP systems

  • Good interpersonal, team, and collaborative skills are a must

  • Excellent oral and written communication skills

WhySandoz?

GenericandBiosimilarmedicinesare the backbone of the globalmedicinesindustry. Sandoz, a leader in thissector,touchedthelivesofalmost500million patientslast year andwhilewe areproudof thisachievement, we have an ambition to domore!

Withinvestmentsin newdevelopmentcapabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have theopportunitytoshapethe future of Sandoz and help more patients gainaccessto low-cost, high-qualitymedicines,sustainably.

Ourmomentumand entrepreneurial spiritispoweredby an open, collaborative culturedrivenby ourtalentedandambitiouscolleagues,who, in return forapplyingtheirskillsexperiencean agile andcollegiateenvironmentwithimpactful, flexible-hybridcareers,wherediversityiswelcomedandwherepersonalgrowthisencouraged!

The futureisours toshape!

FR : Dans le cadre de sa politique Diversité, Evotec étudie, à compétences égales, toutes les candidatures dont celles des personnes en situation de handicap.

ENG : In the frame of our Diversity policy, Evotec considers, with equal competences, all applications including people with disabilities.

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