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Quality Manager

Halma plc
Posted 15 days ago, valid for 14 days
Location

Mentor, OH, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • Volk is seeking a Quality Manager to lead and develop their Quality team, focusing on accountability, collaboration, and continuous improvement.
  • The role requires a Bachelor's degree in Engineering and a minimum of 5 years of experience in quality engineering or management within a regulated manufacturing environment.
  • Key responsibilities include maintaining and improving the Quality Management System (QMS) in compliance with ISO 13485 and FDA regulations, as well as leading internal and external audits.
  • Candidates should have strong knowledge of medical device compliance, CAPA processes, and risk management methodologies.
  • Salary details are not provided in the job listing.

 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!

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
  • Analyze quality data and trends to identify improvement opportunities; develop and report quality metrics to leadership to ensure visibility and accountability

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 #LI-MF2

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By applying, a Halma plc account will be created for you. Halma plc's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.