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.