Quality Systems Specialist
We are thrilled to present an exciting career opportunity as a Quality Systems Specialist, inviting you to join a leading medical devices manufacturing business located in the dynamic north-west region. This role offers an exceptional chance for professional growth within an expanding organization that prides itself on fostering an outstanding work culture.
As a pivotal member of our team, you will play a vital role in ensuring the highest standards of quality and regulatory compliance within our cutting-edge operations. Reporting directly to the esteemed Quality Operations Team Lead and working collaboratively with the Operations Quality Manager, you will have the chance to make a significant impact on the company's success while enjoying a supportive and nurturing work environment.
At our company, we are committed to excellence and innovation, and we recognize that our employees are the driving force behind our achievements. With a clear path for career progression and access to continuous learning opportunities, you will have the tools and support needed to reach new heights in your professional journey.
If you are passionate about quality assurance, eager to be part of a dynamic and forward-thinking team, and ready to take your career to the next level, we encourage you to apply for the role of Quality Systems Specialist. Come aboard and embark on a fulfilling and rewarding career with us as we revolutionize the medical devices industry together.
The key responsibilities in this role are:
Investigate, document and remediate Quality issues that arise within the sites operations and testing areas; communicate and escalate as required
Support Operations to make Quality / Compliance decisions on product during processing, manufacturing, testing, monitoring and packaging
Deliver the quality message around site through team training, presentations and toolbox talks
Metric, pulling together and presenting Quality metrics for the Libre production processes, OpEx, Class A, Gemba, etc.
Support the monitoring and compliance of the Quality Management System as it applies to site Operations.
Plan, conduct and review inspections for all areas as per the inspection plan. Communicate findings and work with area leads to implement corrective actions
Promote a “right first time” approach to Quality Records by ensuring accountability for functional responsibilities
Quality SME for the Libre and BGM manufacturing processes
Education and Years’ Experience:
Relevant third level qualification. Engineering/Manufacturing/Science is preferred.
Minimum 2 years in an Engineering/Manufacturing/Scientific work environment with emphasis on Quality Operations.
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For a confidential discussion and more information on the role, please contact Davin Ferguson