Quality Manager
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Before you apply
LocationMentor
Typefull-time
SenioritySenior
Experience5+ yrs
DepartmentQuality
Company size10,000+ people
PostedAug 27, 2026 · 2mo ago
Verified live3d ago
At a glanceSummarised by Seekless from the posting.
Lead and develop the Quality team
Lead, maintain, and continuously improve the QMS in compliance with ISO 13485, FDA Quality System Regulations (21 CFR §820), and applicable global regulations
Serve as Management Representative for ISO and certification audits
Experience in medical manufacturing
Analyze quality data and trends to identify improvement opportunities
Develop and report quality metrics to leadership
Bachelor's degree in Engineering (Electrical, Biomedical, Chemical, Industrial, or related field)
5+ years of experience in quality engineering or quality management within a regulated manufacturing environment
Strong knowledge of ISO 13485, FDA Quality System Regulations (21 CFR §820), and medical device compliance requirements
Experience with CAPA, nonconformance investigations, and root cause analysis methodologies
Knowledge of design controls, risk management (FMEA), verification, and validation processes
Experience supporting audits and regulatory inspections
Strong analytical, problem-solving, and data-driven decision-making skills
Ability to work cross-functionally and influence outcomes at multiple levels of the organization
Advanced degree preferred
About the company
Volk is the world’s leading brand in ophthalmic diagnostic and surgical lenses. Our purpose is to eradicate preventable blindness through all aspects of the work we do. Volk is a highly regarded, global organization and is a subsidiary of Halma, a FTSE 100 company. To support our ongoing growth, we are looking for you!
Responsibilities
PRIMARY PURPOSE
•
Lead and develop the Quality team, fostering a culture of accountability, collaboration, and continuous improvement aligned with Volk Values
•
Lead, maintain, and continuously improve the QMS in compliance with ISO 13485, FDA Quality System Regulations (21 CFR §820), and applicable global regulations
•
Serve as Management Representative for ISO and certification audits, leading all internal and external audits, including ISO, FDA, and customer audits; experience in medical manufacturing
•
Analyze quality data and trends to identify improvement opportunities; develop and report quality metrics to leadership to ensure visibility and accountability
Requirements
REQUIRED QUALIFICATIONS
•
Bachelor’s degree in Engineering (Electrical, Biomedical, Chemical, Industrial, or related field); advanced degree preferred
•
5+ years of experience in quality engineering or quality management within a regulated manufacturing environment
•
Strong knowledge of ISO 13485, FDA Quality System Regulations (21 CFR §820), and medical device compliance requirements
•
Experience with CAPA, nonconformance investigations, and root cause analysis methodologies
•
Knowledge of design controls, risk management (FMEA), verification, and validation processes
•
Experience supporting audits and regulatory inspections
•
Strong analytical, problem-solving, and data-driven decision-making skills
•
Ability to work cross-functionally and influence outcomes at multiple levels of the organization
•
#volk
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