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Project Automation Area Lead

  1. North America, United States
Ohio
  1. Contract
Competitive
  1. CAPEX Projects
36888
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Project Automation Area Lead - Ohio, United States - 12 Months Contract

This is a fantastic opportunity for a Project Automation Area Lead to join our major, global pharmaceutical client on their latest new-build project based in Ohio, this is a large-scale greenfield capital project and investing more than $1bn.

Responsibilities:
  • Technical ownership for an area in a project
  • Define the S88 software structure and list for the area
  • Develop draft function design specifications for the area
  • Work with system integrators to finalize the functional specifications
  • Participate in P&ID and control strategy reviews
  • Working closely with the Project Technical Lead and System Integrator to successfully deliver the project on schedule and budget
  • Collaborate with Program technical offices to ensure the automation solution is aligned with the overall program automation philosophy and standards
  • Ensure consistency of the automation deliverables in the area (requirements, functional specifications, control strategies, phases, and recipes, etc.)
  • Assist in defining the software components that need to be created or modified
  • Communicate progress, issues, and needs to automation technical lead for the project
  • Provide input, review, and approve functional requirements and specifications
  • Develop Parameter and Recipe Specification documents
  • Responding to system integrator technical queries
  • Identification of any remediation effort required on process control software
  • Create items in the issue tracker as issues arise after the software acceptance
  • Identify and analyze risks of technical nature particular to the area and planning responses
  • Maintain compliance with training requirements
Skills and Experience:
  • BS Engineering (or equivalent experience)
  • Extensive Automation experience in the Pharmaceutical Industry (preferable in API/bulk manufacturing)
  • Previous Pharmaceutical Automation Large Project/Program experience/expertise
  • Extensive experience in DeltaV Batch DCS
  • Preferable, previous experience with Allen-Bradley PLCs
  • Exceptional teamwork abilities
  • Strong knowledge of GMP’s, regulatory requirements and computer system validation principles
  • Excellent written and verbal communication skills for both technical and non-technical audiences
  • Strong knowledge of GMP’s, regulatory requirements and computer system validation principles
  • Excellent written and verbal communication skills for both technical and non-technical audiences
If this role is of interest, please apply now!
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