to join our Quality team. In this role, you will drive corrective actions, support quality system initiatives, and champion continuous improvement across the organisation. You'll work closely with internal teams and external customers to ensure high standards of quality and compliance are consistently met.
Key Responsibilities
Act as a company ambassador, promoting a positive image internally and externally.
Lead investigations into non-conformances, ensuring timely containment and corrective actions using 8D, 5Y, and Ishikawa methodologies.
Collaborate with cross-functional teams to resolve quality issues and implement preventive measures.
Develop and implement Master Validation Plans and Quality Control Plans for new products.
Conduct process capability reviews using SPC techniques and run Gage R&R studies.
Support the creation of FMEAs and perform internal audits.
Assist with inspections across production, manufacturing, and supplier processes.
Maintain accurate quality records and contribute to QMS documentation improvements.
Promote and participate in Continuous Improvement (CI) and Kaizen initiatives.
Work towards personal and team KPIs aligned with departmental goals.
What We're Looking For
HNC or higher in Mechanical, Quality, or related Engineering discipline.
Experience with ISO13485 and medical device standards.
Proficiency in SPC techniques and Gage R&R.
Green Belt certification (preferred).
Internal auditing experience.
Strong analytical, communication, and interpersonal skills.
Proficiency in Microsoft Office and data analytics.
Experience with CMM (preferred but not essential).
A proactive, problem-solving mindset.
Job Types: Full-time, Permanent
Pay: 30,000.00-40,000.00 per year
Additional pay:
Bonus scheme
Quarterly bonus
Benefits:
Additional leave
Company pension
Cycle to work scheme
Enhanced maternity leave
Free parking
Health & wellbeing programme
Life insurance
On-site parking
Private medical insurance
Profit sharing
Referral programme
Sick pay
Schedule:
Monday to Friday
No weekends
Application question(s):
Do you have experience with ISO13485 and medical device standards?
Work Location: In person
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