DeltaV Automation Area Lead (Pharmaceutical Manufacturing)
Location: Flexible (site-based with travel requirements)
Travel: ~4 days/month to Indianapolis, USA
Overview
We are seeking an experienced Automation Area Lead (DeltaV) to take technical ownership of automation delivery within a major pharmaceutical manufacturing program. This role is ideal for someone who has led large-scale pharma automation workstreams end-to-end - owning not just configuration, but architecture, standards, and long-term maintainability across a defined process area.
What Makes This Role Different
- Owned entire automation areas or workstreams on complex, multi-unit facilities
- Led cross-functional coordination (process, utilities, validation, IT/OT, etc.)
- Been accountable for S88 structure, system architecture, and governance decisions
- Delivered projects from early design through configuration and validation
Key Responsibilities
- Take technical ownership for an automation area within a large-scale project
- Define and govern the S88 batch architecture, software structure, and standards
- Develop and review Functional Design Specifications (FDS)
- Collaborate with system integrators to finalize functional design and implementation
- Participate in P&ID and control strategy reviews
- Ensure alignment with program-level automation standards and philosophy
- Oversee consistency across deliverables (requirements, phases, recipes, control strategies)
- Define required software components and modifications
- Support parameter and recipe specification development
- Manage technical queries from system integrators
- Identify risks, issues, and remediation activities related to process control software
- Track and manage post-acceptance issues
- Communicate progress, risks, and technical decisions to project leadership
Required Experience & Skills
- 8+ years of automation experience within the pharmaceutical industry
- Strong experience in API or bulk manufacturing environments preferred
- Demonstrated leadership as an Area Lead or equivalent on large-scale pharma projects
- Owning full automation scope - not just contributing to predefined systems
- 5+ years of hands‑on DeltaV Batch (DCS) experience
- Including design and configuration
- Proven experience delivering projects from early design through build and validation
- Strong knowledge of: S88 batch standards, GMP and regulatory requirements, Computer system validation (CSV)
- Ability to collaborate effectively across multidisciplinary teams
- Excellent communication skills for technical and non-technical stakeholders
- Experience with Allen-Bradley PLCs is a plus
Key Success Factors
- Ownership at area/architecture level, not just system execution
- Ability to define and govern automation standards, rather than simply follow them
- Strong DeltaV batch expertise, including real project leadership experience
- Experience managing full lifecycle delivery (design → configuration → validation)
- Confidence operating in large, complex, multi-disciplinary programs