Process Automation/CSV engineer

Join Realdev’s innovative team where your expertise contributes to groundbreaking projects in pharmaceutical automation.

We are looking for a driven professional eager to make an impact in a dynamic environment.

As the ideal candidate, you are an experienced Senior CSV Engineer with a passion for automation systems. You are communicative, proactive, and constantly seeking improvements. If you are detail-oriented, technically skilled, and enthusiastic about automation, this role might be the perfect fit for you.

What You’ll Do:

• Define, execute, and document Computer System Validation (CSV) activities in compliance with GMP guidelines.
• Create and update the CSV documents (including VPP, SRA, FRP, DRA)
• Test, qualify, and validate process automation systems, including DeltaV and/or PCS 7, OSI Pi Systems.
• Analyze system changes and assess their impact on validation.
• Coordinate validation activities with internal and external stakeholders.
• Actively contribute to the optimization of automation processes.
• Serve as the technical point of contact on the shop floor.

What You’ll Need:

• At least 6 years of experience in CSV within a GMP-regulated environment.
• In-depth knowledge of DeltaV and/or PCS, OSI Pi systems.
• Experience with automation in pharmaceutical manufacturing is a strong asset.
• Excellent communication skills.
• Strong analytical, structured, and pragmatic approach.
• French & English
• Use of KNEAT tool preferred