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Sr Manager Process Analytics & Automation
Posted on Jan. 19, 2026
- Toulouse, France
- 0 - 0 USD (yearly)
- Full Time
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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
Why Sandoz?
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more!
With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!
The future is ours to shape!
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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