Quality Engineer-Medical Devices
- Galway
- Permanent
- Full-time
Purpose: To support a critical site-wide remediation program following an FDA 483 observation.This role offers a fantastic opportunity to work directly onsite, collaborating closely with manufacturing and quality teams to drive compliance improvements and process validation initiatives.
Hours of work: Monday-Friday 39hr week with a 1pm Friday finish.Key Responsibilities:
- Partner with manufacturing process owners to identify and remediate compliance gaps.
- Support manufacturing process validation activities (IQ/OQ/PQ).
- Update quality system documentation and technical files to ensure audit readiness.
- Drive closure of CAPAs and NCRs with effective corrective actions.
- Provide clear and concise technical writing for quality and manufacturing procedures.
- Collaborate cross-functionally with Quality, Manufacturing, and Regulatory teams to implement compliant solutions.
- Bachelor's degree in Engineering or Quality-related discipline.
- 2-5 years of experience in medical device manufacturing, quality, or remediation projects.
- Strong knowledge of process validation (IQ/OQ/PQ) and CAPA/NCR management.
- Proven technical writing and documentation skills.
- Familiarity with 21 CFR Part 820 and ISO 13485 quality standards.
- Excellent problem-solving skills with the ability to take a problem statement through to a compliant solution.
- Must be available to work onsite in Galway.