If you have 3+ years of experience as a Manufacturing Engineer in the medical device industry and you're looking for a fresh, hands-on challenge, this could be the perfect project for you.
We're partnering with a leading Medical Device manufacturer based in Cork, seeking a proactive and detail-oriented Manufacturing Engineer to join their team on a 12-month contract. This is a fantastic opportunity to contribute to cutting-edge process development and work closely with cross-functional teams in a dynamic, high-impact environment.
Key Responsibilities:
- Lead process development, characterisation, qualification, and validation activities for new and existing products.
- Translate project goals into actionable deliverables in collaboration with the Project Manager.
- Provide regular updates on project status, performance metrics, and potential risks to stakeholders.
- Participate in Design for Manufacturability (DFM) reviews with the Design Team to optimize lifecycle costs and ensure robust production processes.
- Ensure all work is conducted with a strong focus on Health, Safety, and Environmental standards.
- Adhere strictly to company procedures and documentation requirements as outlined in the SOP manual.
Requirements:
- Bachelor's degree in Engineering or a related discipline.
- Minimum of 3 years' experience in a regulated manufacturing environment, ideally within medical devices.
- Proven experience in product and/or process development, with a strong understanding of validation methodologies.
- Familiarity with medical device quality and regulatory systems (e.g., ISO 13485, FDA).
- Excellent problem-solving skills, strong communication abilities, and a collaborative mindset.
