Key ResponsibilitiesCoordinate 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 & RequirementsMinimum 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.INDFRS2