Senior Automation Engineer

PerkinElmer is a leader in scientific solutions with a mission of innovating for a healthier world. The Senior Automation Engineer provides expertise in the design, implementation, and lifecycle management of automation systems across biologics and pharmaceutical manufacturing facilities, ensuring client satisfaction through successful project delivery.

Responsibilities:

• Develop full automation system architectures for biologics, pharmaceutical, and advanced therapy manufacturing (DCS, PLC/SCADA, MES, historians, network layers, field instrumentation)
• Create ISA‑88/ISA‑95‑aligned architecture diagrams, I/O strategies, network topologies, and interface specifications
• Ensure architecture supports scalability, cybersecurity, data integrity, and multi‑product flexibility
• Lead the creation, review, and approval of: URS (User Requirements Specifications), FRS (Functional Requirements Specifications), DS / DDS (Design Specifications), Functional & Control Narratives, Recipe Design Documentation (ISA‑88 compliant), Automation Standards & Engineering Guidelines
• Work cross functionally to translate process requirements into robust automation design documents
• Configure, program, and deploy DeltaV DCS (modules, phases, recipes, batch strategies, graphics, alarms)
• Develop, modify, and test Rockwell PLCs (ControlLogix, CompactLogix), FactoryTalk, PlantPAx, and SCADA/HMI applications
• Support integration of OEM skids: bioreactors, chromatography systems, filtration skids, CIP/SIP, and fill finish equipment
• Detailed knowledge of FAT, SAT, IQ/OQ, and PQ protocols in alignment with GAMP 5 and 21 CFR Part 11
• Ensure automation changes meet data integrity requirements, change control processes, and validation lifecycle rules
• Lead deviation investigations, CAPAs, and risk assessments related to automation systems
• Serve as SME for troubleshooting, system optimization, alarm tuning, batch failure analysis, and performance enhancements
• Support 24/7 operations through structured root cause analysis and resolution of automation issues
• Develop long-term automation lifecycle plans for upgrades, patches, and system expansions
• Collaborate with IT/OT, process engineering, quality, and capital project teams to deliver integrated automation solutions
• Manage vendors, system integrators, and OEMs; review design packages and ensure alignment with internal standards
• Mentor junior engineers and act as technical SME during audits and regulatory inspections

Requirements:

• Bachelor's degree in Engineering (Automation, Electrical, Chemical, Mechanical, or related)
• Minimum 9-12+ years in automation engineering within GMP life sciences (biotech, pharma, ATMP)
• Expert-level experience with DeltaV DCS and/or Rockwell / Allen Bradley PLC/SCADA platforms
• Proven ability to author, interpret, and own URS/FRS/DS documentation
• Experience designing system architectures across DCS, PLCs, SCADA, MES, OSI-PI and/or other historians and data systems
• Strong understanding of ISA‑88 batch control, ISA‑95 manufacturing hierarchy, and GAMP 5
• Hands-on experience supporting biologics and sterile/aseptic manufacturing environments
• Understanding multisite standards for global manufacturers
• Willing to travel domestically to meet client project requests
• Experience in professional services or consulting industry highly preferred
• Strong communicator and influencer across engineering, quality, IT/OT, and manufacturing
• Structured thinker with advanced troubleshooting and problem-solving skills
• Skilled at managing multiple priorities in a high pressure, regulated environment
• Ability to manage scope and track project changes
• Demonstrated leadership and mentorship abilities