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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