Delta V Engineer

Key Responsibilities

• Coordinate the development of automation software and hardware to meet New Product Introduction schedules, including FATs, SATs, commissioning, and validation.
• Develop and implement automation solutions in line with S88 batch process standards.
• Deliver robust, compliant, and cost-effective automation solutions within agreed timelines for capital projects.
• Support the Commissioning, Qualification, and Validation (CQV) teams during DeltaV software shakedown and verification.
• Design, code, and test DeltaV software changes identified during commissioning.
• Collaborate closely with other Automation Engineers to ensure milestones are met and standards/library modules are consistently applied.

Qualifications & Requirements

• Minimum 3 years' DeltaV experience on-site in a pharmaceutical environment.
• Strong experience designing and programming control systems with emphasis on DeltaV DCS.
• Knowledge of S88 batch process control in the (Bio)Pharma sector.
• Ability to troubleshoot hardware configurations, operator interfaces, and databases.
• Familiarity with GMP standards; knowledge of 21 CFR Part 11 is a plus.
• Experience in commissioning and start-up of control systems.
• Strong interpersonal and teamwork skills.
• Ability to work effectively in fast-paced, project-driven environments.
• Experience with PLC, HMI, SCADA, and process instrumentation is advantageous.

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