We’re Hiring: Quality System Engineer – Castlebar, Co. Mayo

This person will play a key role in enhancing our Quality Management Systems and supporting the production of life-saving medicines and therapies across the globe.

Why this role?

You’ll work alongside a talented, cross-functional team to drive improvements, ensure compliance, and help shape a culture of quality in a fast-growing environment. This is more than just a QA position—it’s an opportunity to do work that truly matters.

Location: Castlebar, Co. Mayo

Experience: 3+ years in a Quality Assurance role within pharma or biotech

Ideal background: Science, engineering, or business degree preferred

Key Responsibilities

Serve as a quality SME to support and enhance QMS processes in compliance with internal standards and client expectations.
Track and report on QMS metrics and key performance indicators.
Participate in and support Client audits, including resolution of findings and implementation of corrective actions.
Lead the internal audit program: plan schedules, review findings, and track follow-ups.
Drive continuous improvement initiatives and support value-added enhancements across QA functions.
Oversee document control processes and act as site lead for SOP and training compliance.
Coordinate and manage site training programs, aligning with corporate standards.
Collaborate cross-functionally to deliver innovative QA solutions and ensure high performance culture.
Assist in other duties as required to support quality operations.

What we’re looking for:

Detail-oriented with strong problem-solving skills
Self-motivated and results-driven
Excellent communicator with internal teams and external pharma clients
Comfortable working in a fast-paced, cross-functional setting
Willing and able to travel occasionally for business

If you're a QA professional ready to take the next step in your career—and want to be part of something that has a real-world impact—let’s connect.

To learn more, apply, or reach out directly to [email protected]

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