Automation Engineer - Morgan McKinley

apartmentMorgan McKinley placeCork calendar_month 

A leading pharmaceutical company in Cork is seeking an experienced Automation Engineer to support a range of control system initiatives over a 12-month contract. The successful candidate will contribute to the setup and optimization of automation systems, ensuring ongoing compliance and performance improvements across manufacturing operations.

Key Responsibilities:

  • Support the installation and commissioning of automated equipment and control solutions, identifying reliability concerns and upgrade opportunities.
  • Draft and manage documentation related to automation requirements, aligning with project goals, maintenance schedules, and process enhancements.
  • Perform compliance reviews and audits to ensure alignment with industry regulations and identify any areas needing corrective action.
  • Deliver high-quality automation outputs on schedule, tracking milestones and coordinating with key stakeholders.
  • Evaluate project scope changes and supply detailed insights to support potential claims related to timeframes or budget.
  • Liaise with technical experts to ensure consistent progress and alignment on project deliverables both within the organization and externally.
  • Provide mentorship and guidance to junior engineers, fostering knowledge transfer and professional development.
  • Act in accordance with Johnson & Johnson's values and leadership standards during all team and project interactions.
  • Promptly report business issues or improvement opportunities to the appropriate leadership level.
  • Follow all applicable Health, Safety, and Environmental protocols as defined by the company.
  • Ensure strict compliance with regulatory and internal standards across all assigned tasks.
  • Carry out additional duties as needed in support of broader team objectives.

Qualifications & Skills:

  • Minimum of 2 years' experience in automation engineering within the life sciences or a closely related industry.
  • Degree-qualified in Engineering, Science, or a relevant technical field.
  • Proficient in PLC programming and automation project execution.
  • Skilled at reading and interpreting technical schematics and engineering documentation.
  • Understanding of quality standards and regulatory frameworks in medical device or pharmaceutical manufacturing environments.

Preferred Experience:

  • Familiarity with computer system validation processes.
  • Exposure to manufacturing execution systems and related technologies.
  • Competence in managing and configuring databases.
  • Knowledge of IT network infrastructure in industrial settings.
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