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People Power for an Autonomous Age

In the ever-advancing world of AI, the real game changers are the humans behind the algorithms.

What we do

We provide exceptional talent, armed with the precise skills required to architect and implement AI & Data solutions that empower organisations to shape their future.

Mission

Transforming AI & Data from buzzwords into your business’s most valuable asset.

At Generative, we know technology is far more than writing code. It’s about people who dare to dream big – and who can turn those dreams into reality. Whatever your AI & Data ambitions, we'll connect you with talent that understands your vision and has the skills to make it happen.

Talent solutions

Permanent

Securing top talent is crucial for your business's growth and advancement in AI & Data skills.

Flexible

AI’s always advancing, and our network of agile, skilled professionals is here to keep you at the forefront.

Fractional

Fractional AI experts for instant people power

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Job Openings

DeltaV Batch Lead

Raleigh, NC, USA
Up to $110 an hour
Interim
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.

CSV Engineer

Northern Ireland, UK
Up to 70 EUR an hour
Interim
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.

DeltaV Engineer

Northern Ireland, UK
Up to 70 EUR an hour
Interim
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
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Why Us?

Expertise Armed with the Precise Skills

If you’re looking for a partner who can help you reach your AI goals, let’s talk. Because in an autonomous age, it's human connections that make all the difference.