Automation Engineer - QBMS

Evotec; Toulouse; Sur place; EUR 45 000 - 65 000; Plein temps

Résumé du poste

A leading life sciences organization in Toulouse is seeking an Automation Engineer QBMS to lead the configuration and implementation of Building Management Systems. This role requires 5+ years of experience in the pharmaceutical or biotech field and proficiency in automation and instrumentation. Candidates should have strong attention to detail and excellent communication skills in both English and French, and will support compliance with regulatory standards. Opportunities for growth and a collaborative culture await you.

Prestations

Growth Opportunities

Flexible Work Environment

Inclusive Culture

Qualifications

• 5+ years relevant experience in pharmaceutical or biotech fields.
• Strong control system automation background.
• Experience working in a GMP environment.

Responsabilités

• Lead configuration of Building Management Systems.
• Support design and development of automation solutions.
• Collaborate with the validation team for regulatory compliance.

Connaissances

Control system automation

Strong attention to detail

Interpersonal and communication skills

English and French proficiency

Formation

Automation Engineering or related field

Outils

PCVue

Siemens PLC

TIA Portal

DeltaV

Description du poste

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 challenge …in our journey

We’re looking for a passionate and curious Automation Engineer QBMSto 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.

The Automation Engineer will be part of the JPOD2 Automation team in the MTS/MSAT department. The incumbent will serve as the site-level lead for the configuration, implementation, validation, and lifecycle management of the site Building Management Systems for a clinical and commercial manufacturing site at the Toulouse J.POD manufacturing facility. The successful candidate will have demonstrated proficiency in Automation and Instrumentation Design and Validation, Systems integration using industry standard protocols (BACnet, Profinet, OPC, Hart) with related business and automation systems, and an understanding of ISA-95 Operational Technology architecture. Experience working in a GMP environment, change control, and software validation in accordance to GAMP5 guidelines is required.

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
• Candidate must possess strong focus on quality and attention to detail
• 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 about thinking outside the box—we throw the box away. If you’ve got ideas, we want to hear them.

Are You Still Curious?

If you’ve read this far, then chances are you’ve got a curious mind—just like us. So, what are you waiting for? Take the leap and apply today. We can’t wait to see where your curiosity leads you—and how it will shape the future of Just Evotec Biologics.

Let your curiosity guide your career—#BeCUREious and explore the endless possibilities at Just Evotec Biologics !

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.