Automation Engineer

Job Title: Automation Engineer QBMS

Location: Toulouse
Department: : Automation
Reports To: Sr Automation Engineer

About Us: this is who we are

At Just Evotec Biologics, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what’s possible. We're on a mission to create a place where curiosity isn't just encouraged—it’s celebrated.

Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCUREious with us and see where your curiosity can take you

The Role: Your challengein our journey

We’re looking for a passionate and curious Automation Engineer QBMS to join our team. If you’re excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories.

As a Automation Engineer QBMS at Just Evotec Biologics, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It’s a role where your curiosity will fuel both your personal growth and the success of the team.

What You’ll Do:

- Serve as the site-level lead or support for the configuration, implementation, validation, and lifecycle management of the site Building Management Systems.
- Support the definition of equipment and User Requirements
- Support the Design and Development of the Building Automation Solutions
- Evaluate new equipment and new technologies prior to implementation
- Maintain compliance with company standards.
- Define maintenance requirements and spare parts management
- Participate in impact assessment for equipment/system failures
- Develop and implement lifecycle documentation for the BMS system including user requirements, design and functional specifications, SOPs, training documents, etc.
- Collaborate with the validation team for the initial and ongoing qualification of the QBMS system and related instrumentation. Ensure full regulatory compliance including requirements for GMPs and data integrity.
- Provide on-demand technical support including troubleshooting and issue resolution related to Automation system infrastructure, configuration and interfaces to support operational requirements.
- Lead or contribute to technical root cause analysis, incident investigations, and troubleshooting of process control issues.
- Provide project oversight on BMS implementation projects contracted to vendors or 3rd party suppliers/integrators.

Who You Are:

- Automation Engineering, Electrical Engineering, Computer Science, Chemical Engineering, Biotech Engineering or related life science engineering.
- Experience with PCVue, Siemens PLC, TIA Portal platforms
- 5+ years relevant experience in pharmaceutical, biotech, or life sciences with 5+ years of experience with current Good Manufacturing Practice (cGMP) regulations
- Strong control system automation background including design, installation, programming and validation of automated processes
- Working knowledge of cGMP manufacturing and regulatory regulations and requirements (FDA CFR 21 Part 11 and EMA Annex 11) for biologics/pharmaceuticals
- Leverage experience of Good Automated Manufacturing Practice (GAMP) framework for risk-based approach to computer system validation
- Established record of successful project completions employing proven engineering skills
- Demonstrated skills coding in Siemens Platforms (TIA Portal)
- Demonstrated skills developing HMI and SCADA (PCVue, WinCC)
- Demonstrated skills designing and integrating instrumentation in BMS
- Good interpersonal, team, and communication skills are a must
- Excellent oral and written communication skills in both English and French
- Experience in computer software validation in both writing test scripts and executing test protocols is strongly preferred
- Experience using GAMP5 risk-based approach when implementing changes to validated software systems
- Experience in supporting audits and inspections by health authorities and other external auditors
- Experience with DeltaV

Proficiency developing and executing CSV plans and protocols

Why Join Us:

- Growth Opportunities: We’re a company that believes in continuous learning and development. Whether it’s professional courses, mentorship, or new projects, we’ll help you grow.
- Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life.
- Inclusive Culture: We’re committed to building a diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged.
- Innovative Projects: You’ll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.
- A Place for Big Ideas: We don’t just talk abou