Senior Supplier Quality Engineer - Medical Devices

CORIN LIMITED; Cirencester; On-site; GBP 40,000 - 45,000; Full time

Benefits offered by this job

Discretionary annual bonus of 7.5%

Pension

Private medical insurance with family

Eye tests & flu vaccinations

Employee referral program

Job summary

CORIN LIMITED in Cirencester seeks an experienced Supplier Quality Engineer to ensure supplied parts meet manufacturing specs and regulatory standards. You will collaborate with suppliers and cross-functional teams to drive defect prevention, CAPA, and continuous improvement throughout the supply chain.

The role emphasizes supplier audits, eQMS management, CAPA closure, and supporting medical device compliance (ISO 13485, FDA 21 CFR Part 820, GMP).

Qualifications

• Degree or equivalent practical experience in engineering/science.
• 5+ years in a Quality Engineering role in manufacturing/mechanical env.
• Experience in supplier quality management and medical devices.
• Knowledge of ISO 13485, FDA 21 CFR Part 820, GMP and CAPA.

Responsibilities

• Collaborate with suppliers to implement defect prevention and continuous improvement.
• Lead root-cause investigations and corrective actions to minimise disruption.
• Manage supplier non-conformances through eQMS and CAPA systems.
• Provide technical support to suppliers ensuring customer-specific requirements.
• Drive supplier development initiatives and support NPI ensuring process robustness.

Skills

Problem-solving

Root cause analysis

Communication

Stakeholder management

Education

Degree in Engineering, Science, or related discipline

Tools

eQMS

Job description

CORIN LIMITED in Cirencester seeks an experienced Supplier Quality Engineer to ensure supplied parts meet manufacturing specs and regulatory standards. You will collaborate with suppliers and cross-functional teams to drive defect prevention, CAPA, and continuous improvement throughout the supply chain.

The role emphasizes supplier audits, eQMS management, CAPA closure, and supporting medical device compliance (ISO 13485, FDA 21 CFR Part 820, GMP).