DeltaV Batch Lead

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.

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