Quality Engineer (Hybrid)

Galway's world leading medical device manufacturing company have available opportunities for EXPERIENCED Quality Engineers to join their team. Please send CV to [email protected] or call Gary on 0861030418 to apply.
 
About the role:
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.  Hybrid role offering 2 days work from home.
 
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.

Qualifications & Experience:

• 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.

INDCRG