
Automation Engineer II
Lessines, WalloniaOn the Global Manufacturing and Supply (GMS) team at Takeda, you’ll be part of a rapidly transforming industry that’s applying technology and data in new ways. Within our agile, innovative, people-centric organization, your work will matter every day as you use your skills to help us manufacture therapies for patients on our four platforms:
- Small Molecules
- Biologics
- Plasma
- Cell and Gene
As part of the GMS team, you'll have the opportunity to pursue unique experiences and build new skills, and you'll know that the work you do every day makes an impact — on our patients, our people, our planet, and on yourself.
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Job Description
Automation Engineer II
The Automation engineer II is integrated in the automation structure.
Automation Engineering is the core foundation for OT Shopfloor Systems & Data Access and as such a key element to introduce Industry 4.0 to provide shopfloor data for data science & analytics on industrial scale.
The target of Automation Engineering is that all manufacturing systems are following an end-to-end harmonized way to utilize shopfloor data from a seamlessly integrated & modernized and secure automation system landscape. Shopfloor integration follows an automation standard framework, the automation obsolescence is managed risk-based including cybersecurity & data integrity mitigations and a game-changing speed up of shopfloor data availability & utilization per site materializes.
The manufacturing site of Lessines is composed of purification, filling and packaging lines. Its activities is supported by utilities systems such as a power plant area.
The installation, programmation, configuration and support of those equipment are managed by the automation team.
The automation system consists of Osi-Pi, DCS PCS7, Oracle and SQL databases, drives...
The automation team is split in three area: support, project and strategy.
Depending of the area the scope position is to:
- Be the Technical system support (troubleshooting, improvement) and automation SME to support and implement process, data driven or innovative solution;
- design, installation/modification, commissioning and qualification of automation systems according to EHS, GMP (Good Manufacturing Practices) and GEP (Good Engineering Practices) requirements;
- continuously improve automation process and standard
ACCOUNTABILITIES
The incumbent must be able to manage, without assistance, automation modifications or be integrated in larger projects teams. In particular, the position implies :
Support:
- Technical system support (level 2) for automation
- Reduce automation issues on existing systems (improvement)
- Support investigation by providing automation expertise
- Develop and implement complex change on automation,
- Provide support for the deployment of use case for data, innovation and for AIMP
Projects:
- Prepare future manufacturing project (pre-capex) including:
technical study (internalized or externalized)
Provide automation standard / tender
Project plan preparation (including offer from automation/ engineering partner)
- Follow manufacturing project (capex) including:
provide automation expertise
Partner follow up (technical and documentation)
participation in the project execution and implementation
Strategic activities
- participate in the creation of automation standard
- Work with global automation and local IT to deploy Global automation program and ensure standard approach on all project
- Analyse and Improve the efficiency of the team during change control activities
- Create and deploy automation obsolescence program
Common activities:
- Provide 24/24 7/7 off-site support (level 2)
- Coordinate technically up to 3 automation engineers
Education / experience:
- Master degree in Automation, Electrics: (Or Bachelor degree + Exp.)” with at least 5 years’ experience in automation pharmaceutical domain.
- Comfortable with the technology evolution for automation systems.
Core Competencies / Skills / Leadership Behaviors:
- Good communication skills and the ability to lead and perform effectively in multi-disciplinary teams
- Must have the ability to effectively participate to Engineering projects, coordinate suppliers, and drive results.
- Has the ability to prioritize multiple tasks and work on multiple projects simultaneously.
- Develop his (or her) understanding of business drivers and customer needs.
- GAMP5 Methodology
- Experience with Quality Systems and Processes in a GMP regulated and FDA+Eudralex licensed manufacturing site.
- Must have good experience in project management, preparing project budgets and timelines
- Must be comfortable with MS OFFICE Pack (Especially WORD, POWERPOINT, EXCEL).
- Must be sensitive to Data Integrity aspects.
Locations
BEL - LessinesWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full timeWorking at Takeda
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Empowerment
Through trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.
We're Steadfast In Our Commitment to Four Key Imperatives
Patient
Responsibly translate science into highly innovative medicines and accelerate access to improve lives worldwide.
People
Create an exceptional people experience.
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Data & Digital
Transform Takeda into the most trusted, data-driven, outcomes-based biopharmaceutical company.
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