Production Quality Manager
Permanent
permanent
ENGINEERING
12 Oct 2025
Oxford, England
Verified by Turrior
Content + Source + Freshness • 12 Dec 2025 • 95% confidence
75 / 100
Offer value
Moderate value attributed to a stable position in a regulated industry, with growth opportunities but a set skill requirement for quality control.
- Stable role in quality management for medical devices
- Clear regulatory requirements and responsibilities
- Opportunities for process improvement and leadership
- Requires specific technical skills and experience
Pros
- Good growth opportunities within the medical devices sector
- Stable employment due to regulatory nature
- Opportunity to work with quality management systems
Cons
- Requires specific experience in quality control tools and regulations
- May involve high-pressure situations dealing with compliance issues
- Potentially limited exposure to innovative processes or technologies
Who it's for
Mid to Senior Level • On-site
Good fit
- Mid-senior quality control professionals
- Candidates passionate about quality and compliance
- Individuals with experience in medical or electronics manufacturing
Not recommended for
- New graduates with no relevant work experience
- Professionals uninterested in strict regulatory environments
- Those looking for fully remote work
Motivation fit
Interest in quality assurance and regulatory standardsDrive to contribute to safety and efficacy in medical productsAspiration to lead quality initiatives within a manufacturing context
Key skills
Quality control methodologiesRegulatory compliance knowledgeTeam leadershipData analysis for quality metrics
Score: 75/100 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
