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Tier-1 brand and mid-level role, but specialized automation and regulated manufacturing reduce candidate pool.
Specialized automation, machine-building, and regulated manufacturing experience limits easy transfer across industries.
Requires specific automation, machine-building, validation, and regulated manufacturing experience, making screening highly selective.
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Lead end-to-end delivery of engineering, automation, and custom machine-building projects including planning, design, FAT, SAT, commissioning, qualification, and handover.
Own project scope, schedule, budget, and risk management ensuring compliance with safety, quality, and regulatory standards in a regulated manufacturing environment.
Manage global machine suppliers, OEMs, and system integrators; review and approve design deliverables; and provide technical leadership on PLC, HMI/SCADA, servo drives, vision systems, and electrical instrumentation.
Degree in Electrical, Electronics, Instrumentation, or Automation Engineering preferred.
Strong experience in automation-heavy machine-building or capital project execution with hands-on exposure to global machine vendors/OEMs, PLC programming, servo drives, and vision systems (e.g., Cognex).
Knowledge of machine safety, electrical safety, automation standards, and quality requirements for medical devices/pharma (ISO 13485, FDA 21 CFR Part 820, GMP).
Work Experience Required: Not explicitly mentioned in the JD.
Experienced technical project lead capable of independent hands-on execution in regulated manufacturing (MedTech/Pharma preferred).
Skilled at coordinating cross-functional teams and global vendors with a strong grounding in project management and automation controls.
Demonstrated ability to manage complex machine safety and validation processes including IQ, OQ, PQ and compliance documentation for audit readiness.