Quality Control Manager
Permanent
permanent
ENGINEERING
30 Sep 2025
Oxford, England
Job Opportunity at Engineering Employment
Content + Source + Freshness • 12 Dec 2025 • 95% confidence
85 / 100
Offer value
High value due to significant career impact potential in quality control and regulatory compliance sectors.
- Invaluable role in product quality assurance
- Significant growth potential within the medical industry
- Requires strong knowledge of compliance and quality processes
Pros
- Critical role in ensuring product quality in a regulated industry
- Opportunities for professional development in quality management
- Strong stability from working within established companies and industries
Cons
- Requires comprehensive knowledge of regulatory frameworks
- Potentially high-pressure role due to compliance demands
- May involve long hours during product validation periods
Who it's for
Mid to Senior Level • On-Site
Good fit
- Quality control specialists in the medical device field
- Candidates with robust experience with industry regulations
- Professionals motivated by process improvement
Not recommended for
- Entry-level individuals without experience in quality assurance
- Those uncomfortable with regulatory obligations
- Candidates seeking low-pressure job environments
Motivation fit
Desire to enhance product quality and compliance metricsInterest in continuous improvement methodologies
Key skills
Quality management and assuranceFamiliarity with regulatory standards (ISO, FDA)Analytical skills for data interpretation
Score: 85/100 AI verified analysis
About the job
The Quality Control Manager in the field of Medical Devices or Electronics Manufacturing is responsible for overseeing and managing all aspects of quality control within the organization.
This role involves ensuring that products meet established quality standards and regulatory requirements, identifying and addressing any quality issues, and implementing continuous improvement initiatives to enhance overall product quality and customer satisfaction.
Key skills
Experience with quality control tools and methodologies, such as statistical process control (SPC), failure mode and effects analysis (FMEA), and root cause analysis (RCA) ??? BS EN ISO 14971:2021.
Familiarity with regulatory requirements and quality standards in the medical device industry, such as ISO 13485 and FDA regulations
Issuance of exception documents, such as Non-Conformances and CAPA???s
Generation of Validation and Verification documentation and testing reports.
Experience in performing Internal and External Supplier Audits.
Internal Auditor Trained
