- Type
- Full-time
- Department
- Engineering
- Experience
- 3+ years
- Source
- RecruiterFlow
Description
Réalta Technologies are searching for a skilled DeltaV Automation Engineer to support a biotechnology client of ours on the design, implementation and optimisation of automation systems across their growing GMP facility. The successful candidate will play a key role in supporting system start-up, commissioning, and ongoing manufacturing operations.
Job Responsibilities
- Design, configure, test, and deploy Emerson DeltaV control strategies to support manufacturing operations.
- Support start-up, commissioning and qualification activities for new and existing process automation systems.
- Troubleshoot automation issues and provide hands-on support to operations, maintenance and engineering teams.
- Develop and maintain automation documentation, including functional specifications, configuration standards and test protocols.
- Collaborate with process engineering, quality, and validation teams to ensure automation systems comply with GMP, GAMP 5 and relevant regulatory standards.
- Participate in change control, deviation investigations and continuous improvement initiatives.
- Provide technical input for automation upgrades, system expansions, and integration with MES, historians and other site systems.
Job Requirements
- Bachelor’s degree in Engineering, Automation, Control Systems, or a related discipline.
- 3+ years of experience working with Emerson DeltaV in a biotech/pharma or other highly regulated environment.
- Start-up and commissioning experience strongly preferred.
- Solid understanding of batch processing, S88 standards, and GMP automation best practices.
- Experience writing and executing FAT/SAT, IQ/OQ protocols.
- Strong troubleshooting skills and the ability to work effectively in a fast-paced, cross-functional environment.
- Excellent communication skills with the ability to translate complex automation concepts to technical and non-technical stakeholders.
Skills
GMP
