CREGG are seeking a motivated
Quality Engineer
to join our established Quality team on a Permanent basis.
This is an excellent opportunity to develop your career within a growing company that manufactures products for the
medical technology, ICT, and agri-technology sectors
.
In this role, you will support manufacturing operations by ensuring products, processes, and systems meet internal quality standards and regulatory requirements.
You will work closely with Operations, Engineering, and Supply Chain teams to drive
process improvements, maintain quality systems, and support continuous improvement initiatives
.
Reporting to the
Quality Manager
, you will also collaborate with the wider Quality team, including Quality Inspectors, Incoming Inspectors, and the Quality Technician.
For more information contact Mark: ************ or ******
Key Responsibilities
Process & Product Quality
Provide responsive Quality Assurance support to manufacturing operations.
Drive process improvements to enhance product quality, yield, and process reliability.
Identify opportunities for risk reduction, error-proofing, automation, and cost improvement.
Apply quality tools such as
FMEA, DOE, SPC, and CpK analysis
to monitor and improve process performance.
Track and analyse key quality metrics to identify trends and improvement opportunities.
Quality Systems & Compliance
Support the implementation and continuous improvement of the
Quality Management System (QMS)
.
Ensure compliance with
ISO ****, ISO *****, EU MDR, FDA
, and other regulatory requirements.
Participate in
internal audits, regulatory inspections, and customer audits
.
Manage Engineering Change Orders (ECOs) and support the
QPulse quality management system
, including corrective actions.
Validation & Investigations
Support
process and product validations (IQ, OQ, PQ)
and prepare validation documentation.
Lead or support
root cause investigations
using structured methods such as
8D, 5 Whys, and Fishbone analysis
.
Review customer complaints, analyse trends, and drive corrective actions.
Supplier & Continuous Improvement
Support supplier quality activities and investigations, including
SCARs and supplier performance monitoring
.
Contribute to
Lean manufacturing and continuous improvement initiatives
across the site.
Support product and process transfers from development or other manufacturing locations.
Provide technical support and guidance to members of the Quality team.
Work cross-functionally with Operations, Engineering, and Supply Chain on quality and improvement projects.
Qualifications & Experience
Experience
Minimum
5 years' experience
in a manufacturing environment (medical device or regulated industry preferred).
Experience working with
quality systems and regulatory standards
.
Education
Level 7 or Level 8 qualification
in Engineering, Quality, or a related discipline
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