Manufacturing/Equipment Engineer
We have a current opportunity for a Manufacturing/Equipment Engineer on a contract basis. The position will be based in Cork. For further information about this position please apply.
The contract details are below:
- Duration: 12 months initially (with the potential to extend)
- Location: Based in Cork
- Work Arrangement: 80% onsite
- Hours: 40 hours per week
Key Responsibilities:
- Equipment/Manufacturing background
- Equipment qualification (General Equipment)
- Debugging
- OQ, PQ
- No bespoke Automation
- Problem solving
We are seeking a skilled and proactive Manufacturing/Equipment Engineer to join our dynamic team in the medical devices sector. The ideal candidate will have a strong background in equipment qualification, manufacturing process support, and problem-solving within a regulated environment. This role is critical in ensuring that manufacturing equipment is properly qualified, maintained, and optimised to support high-quality and compliant production.
- Lead and support equipment qualification activities including IQ/OQ/PQ protocols and documentation.
- Collaborate with cross-functional teams to ensure compliance with regulatory standards (e.g., ISO 13485, FDA 21 CFR Part 820).
- Troubleshoot and resolve equipment and process-related issues to minimise downtime and improve efficiency.
- Develop and implement preventive maintenance plans and continuous improvement initiatives.
- Support new equipment installation, commissioning, and validation.
- Maintain accurate and up-to-date engineering documentation, including SOPs, work instructions, and validation reports.
- Provide technical support for process development, scale-up, and transfer activities.
- Participate in root cause analysis and corrective/preventive actions (CAPA).
- Ensure adherence to Good Manufacturing Practices (GMP) and safety standards.
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