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À propos
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Located near Sligo, our global pharmaceutical client is seeking a Quality Engineer to join their state‑of‑the‑art manufacturing facility. The company focuses on investing in research and development to drive scientific innovation and deliver life‑changing medicines. With thousands of employees worldwide and continued growth across their network, this is an excellent opportunity to join a leading organisation shaping the future of healthcare.
What You’ll Do
- Coordinating appropriate assigned elements of the Quality System, ensuring full compliance by all relevant plant personnel with its requirements.
- Audit the quality system with other personnel where required.
- Assist in the investigation and coordination of customer complaints and assess the need for implementation of effective corrective or preventive actions.
- Manage day‑to‑day CAPA requirements by ensuring timely and effective initiation, investigation, correction and corrective actions.
- Measure performance of the Quality System and provide metrics, for inclusion in the management review, monthly reports etc.
What you’ll need:
- Extensive experience in the day‑to‑day operation of the quality system in a highly regulated combination product/device manufacturing environment.
- Extensive working knowledge of quality systems regulations (ISO13485/ISO9000; CFR 21 Part 820) or individual elements within the regulations such as process validation, design controls, CAPA, auditing, etc., is desirable.
- Experience in an injection moulding or tooling environment is desirable. xcfaprz
Apply now to become a part of this life changing project!
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Compétences linguistiques
- English
Avis aux utilisateurs
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