Overview
Skills
Job Details
Catalyx is seeking a DeltaV Automation Lead who will be responsible for the control system solution for an area within a project ensuring the solution is aligned with the overall program automation philosophy, standards and user requirements.
Role 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
Requirements
· BS Engineering (or equivalent experience)
· 8+ years working Automation experience in the Pharmaceutical Industry (preferable in API/bulk manufacturing)
· Previous Pharmaceutical Automation Large Project/Program experience/expertise
· 5+ years’ experience in DeltaV Batch DCS
· Preferable previous experience with Allen-Bradley PLCs
· Strong knowledge of GMP’s, regulatory requirements and computer system validation principles
· 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