Automation

This company is a trusted systems integrator serving the Life Sciences sector, is seeking a DeltaV Batch Lead to support a major pharmaceutical project. This is a 12-month contract opportunity, starting with 3 months on-site in Raleigh, NC, followed by a transition to a fully remote role. This position requires end-to-end DeltaV project lifecycle experience, including commissioning and startup as well as early-stage design and documentation. The successful candidate will have a strong background working within GMP-regulated pharmaceutical environments, with a deep understanding of ISA-88 batch standards. Key Responsibilities Serve as the technical lead for DeltaV Batch implementation across all phases of the project. Oversee and execute commissioning and startup activities on-site during the initial project phase. Lead early-stage design, batch configuration, and documentation development in the remote phase. Collaborate with cross-functional teams including automation engineers, validation, and quality assurance. Ensure compliance with GMP, FDA, and ISA-88 standards throughout all project phases. Troubleshoot system issues and provide guidance during validation and handover processes. Required Experience & Skills Extensive hands-on experience with DeltaV Batch, including configuration, testing, commissioning, and design. Proven track record managing full project lifecycle from design through to startup in a pharmaceutical environment. Deep understanding of ISA-88 (S88) and GMP requirements. Strong documentation skills (URS, FRS, DDS, FAT/SAT protocols). Ability to work independently and remotely, while maintaining clear communication with project stakeholders. Excellent leadership, coordination, and problem-solving abilities.

This company is a leading systems integrator in Ireland, is seeking an experienced CSV (Computer System Validation) Engineer for a 12-month contract based full-time on-site at a pharmaceutical manufacturing facility in Northern Ireland. This is a fantastic opportunity to work on a high-profile project, ensuring the validation of automation systems within a GMP-regulated environment. Key Responsibilities Lead and execute validation activities for automation systems, focusing on DCS/PLC systems within a pharmaceutical manufacturing site. Develop and implement validation documentation including URS, IQ, OQ, PQ, and validation plans. Ensure compliance with regulatory requirements (e.g. GAMP 5, FDA 21 CFR Part 11, EU GMP Annex 11). Perform risk assessments, impact assessments, and deviation investigations. Collaborate with cross-functional teams including automation, quality, and IT departments. Provide support during audits and inspections related to system validation. Required Experience & Skills 4–10 years of experience in Computer System Validation within the pharmaceutical or life sciences sector. Hands-on experience validating DeltaV systems preferred; other DCS or PLC systems will also be considered. In-depth knowledge of GMP, GAMP 5, and regulatory expectations. Proven ability to author, review, and execute validation protocols and reports. Strong problem-solving, documentation, and communication skills. Ability to work independently on-site in a fast-paced environment.

This company is a leading systems integrator in Ireland, is seeking an experienced DeltaV Engineer to join a high-impact pharmaceutical project in Northern Ireland. This is a 12-month contract working fully on-site with a top-tier pharma client, offering excellent day rates and exposure to a regulated GMP environment. Key Responsibilities: Execute full DeltaV project lifecycle activities, including: System design and architecture Software configuration and development FAT/SAT testing On-site commissioning and startup Work within GMP-regulated environments, ensuring compliance with relevant standards and procedures Apply knowledge of ISA S88 batch control standards in system design and implementation Collaborate with cross-functional teams including validation, QA, operations, and project management Troubleshoot and support DeltaV systems during the commissioning and qualification phases Requirements: 4–10 years of hands-on experience with Emerson DeltaV DCS Proven experience across the entire project lifecycle Strong background working in pharmaceutical manufacturing environments In-depth knowledge of GMP regulations and ISA S88 standards Ability to work independently and on-site 5 days per week Excellent communication and documentation skills