Quality Assurance Specialist
We are seeking a highly skilled Quality Assurance Specialist to join our team. This is a 18-month fixed-term position offering hybrid working with a competitive salary and package.
The ideal candidate will be a key member of the Supplier Quality team, reporting to the Senior Quality Engineer. They will play a vital role in ensuring regulatory compliance in area of responsibility to cGMP's, with the ability to train others.
Key Responsibilities:
* Lead/participate in continuous improvement/CAPA team activities
* Perform risk management activities in a cross-functional environment
* Ensure that documentation and work practices comply with ISO and regulatory requirements
* Develop, maintain, and improve the quality management system
* Assess quality management system effectiveness through internal audit and performance review
The successful candidate will have a third-level technical/science qualification plus at least 2 years' experience in the medical device or pharmaceutical industry, preferably within supplier management. Knowledge of quality management systems ISO 13485, GMP is essential.
What We Offer:
* A competitive salary and package
* Hybrid working (3 days in the office and 2 from home)
* Ongoing training and development opportunities