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.