Lead and support automation projects, system integration, and control system lifecycle management in a GMP medical device manufacturing environment.
Collaborate across departments to drive NPI, system qualification, and continuous improvement.
Key Responsibilities: Provide technical/project support for manufacturing and NPIs.Lead control system activities and qualification during project start-up.Integrate new systems with enterprise platforms (MES/ERP/OSI PI).Manage control system lifecycle in compliance with SLC and regulatory standards.Troubleshoot, optimize, and document control system operations.Ensure vendor qualification and documentation standards.Uphold EHS and quality compliance.Requirements: Level 8 Degree or Higher Diploma in a technical field.3+ years in automation within GMP pharma (PLC/HMI/SCADA).Experience with 21 CFR Part 11 compliance and system qualification.Accountability & Leadership: High autonomy; expected to take initiative and deliver results.Provide technical leadership; influence cross-functional teams.Ensure right-first-time execution and regulatory compliance.For a confidential discussionandmore information on the role,please contactKevin Griffin. ****** (021) 2427108
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