Validation Engineer – Medical Devices / Injection Moulding
Location:
Longford, Ireland
Schedule:
Full-time, 5 days on site
We are a
world-leading injection moulding manufacturer
supplying high-quality components to the medical device industry.
Our Longford facility is a high-tech, fast-paced environment where innovation and quality come first.
We are now seeking a
Validation Engineer
to join our team.
This is a hands-on role, working on site 5 days per week, supporting manufacturing operations and ensuring that our processes meet the highest industry standards.
Key Responsibilities:
Plan, execute, and document validation activities including IQ, OQ, and PQ for equipment, processes, and systems.
Carry out
hands-on documentation within validation
, ensuring all protocols, reports, and records are accurate and compliant.
Collaborate with cross-functional teams to ensure compliance with regulatory and quality requirements.
Analyse data and prepare validation reports to support product release and process improvements.
Maintain validation documentation in line with internal policies and industry standards.
Requirements:
Experience in the
medical device
sector
or
in
injection moulding
manufacturing.
Strong understanding of validation principles and regulatory requirements.
Demonstrated experience with IQ, OQ, and PQ protocols.
Excellent problem-solving and communication skills.
Ability to work independently in a fast-paced, highly regulated environment.
Why Join Us?
Be part of a world-class manufacturing operation producing life-saving and life-enhancing products.
Work with cutting-edge technology in a collaborative, supportive environment.
Opportunities for professional growth and development.
If you're a detail-oriented validation professional with a passion for quality and precision, we want to hear from you.
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