Cinova Medical Inc
The Quality Engineer is responsible for supporting and maintaining the Quality Management System (QMS) to ensure compliance with ISO 13485, FDA 21 CFR Part 820, and customer‑specific requirements. This role focuses on the investigation and resolution of product and process nonconformances, managing CAPA and SCAR processes, coordinating MRBs, and ensuring SOPs are properly implemented and followed. The Quality Engineer also plays a key role in preparing for and supporting internal, external, and customer audits. Additional responsibilities include providing training to operators on quality requirements, procedures, and Good Documentation Practices (GDP) to ensure compliance and consistency across manufacturing activities.
Essential Duties and Responsibilities
Support, maintain, and improve the Quality Management System (QMS) to ensure regulatory and customer compliance.
Lead or participate in Corrective and Preventive Action (CAPA) investigations, ensuring thorough root cause analysis, effective corrective actions, and timely closure.
Review and disposition NCRs; coordinate Material Review Boards (MRBs) to drive effective decision‑making on nonconforming materials and parts.
Manage Supplier Corrective Action Requests (SCARs), follow up with suppliers on corrective actions, and ensure customer concerns are resolved promptly.
Draft, revise, and maintain SOPs, work instructions, and quality procedures to ensure consistency, clarity, and compliance.
Act as a key participant in internal audits, customer audits, and third‑party audits; provide documentation, lead audit responses, and ensure timely follow‑up actions.
Track and report on quality metrics such as CAPA trends, SCAR closure rates, NCR frequency, and audit outcomes; provide data‑driven insights to management.
Support lean and Six Sigma initiatives, process validations, and risk management activities to improve product quality and process capability.
Provide training to operators on quality procedures and GDP requirements to ensure proper documentation and compliance.
Qualifications
Bachelor’s degree in Engineering, Quality, or related technical field (or equivalent experience).
2+ years of experience in quality engineering within medical device, pharmaceutical, or regulated manufacturing environment.
Strong working knowledge of ISO 13485, FDA 21 CFR Part 820, and related quality system requirements.
Experience with CAPA, NCRs, MRBs, SCARs, SOPs, and audit preparation.
Excellent documentation, communication, and organizational skills.
Proficient with Microsoft Office; experience with electronic QMS software preferred.
Preferred Qualifications
Experience in injection molding, precision manufacturing, or medical device production.
Experience in Medical Device (ISO 13485) manufacturing industry.
Knowledge of ISO 9001/134855/FDA requirements and compliance.
Familiarity with GD&T, metrology equipment (CMM, optical systems), and statistical analysis tools (Minitab/Excel).
Ability to speak with customers.
Strong problem‑solving and cross‑functional teamwork abilities.
Language Ability
Ability to read, write, understand and follow instructions in the English language.
Effective oral and written communication in the English language.
Spanish is a plus.
Benefits: Medical; Dental; Vision; Life; STD; LTD; 401(k) with company match; Paid Time Off
Cinova Medical, Inc. is an Equal Opportunity Employer and a Drug Free Workplace.
Upon hire, Cinova Medical, Inc. uses E-Verify to verify employment eligibility for roles based in the United States.
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Essential Duties and Responsibilities
Support, maintain, and improve the Quality Management System (QMS) to ensure regulatory and customer compliance.
Lead or participate in Corrective and Preventive Action (CAPA) investigations, ensuring thorough root cause analysis, effective corrective actions, and timely closure.
Review and disposition NCRs; coordinate Material Review Boards (MRBs) to drive effective decision‑making on nonconforming materials and parts.
Manage Supplier Corrective Action Requests (SCARs), follow up with suppliers on corrective actions, and ensure customer concerns are resolved promptly.
Draft, revise, and maintain SOPs, work instructions, and quality procedures to ensure consistency, clarity, and compliance.
Act as a key participant in internal audits, customer audits, and third‑party audits; provide documentation, lead audit responses, and ensure timely follow‑up actions.
Track and report on quality metrics such as CAPA trends, SCAR closure rates, NCR frequency, and audit outcomes; provide data‑driven insights to management.
Support lean and Six Sigma initiatives, process validations, and risk management activities to improve product quality and process capability.
Provide training to operators on quality procedures and GDP requirements to ensure proper documentation and compliance.
Qualifications
Bachelor’s degree in Engineering, Quality, or related technical field (or equivalent experience).
2+ years of experience in quality engineering within medical device, pharmaceutical, or regulated manufacturing environment.
Strong working knowledge of ISO 13485, FDA 21 CFR Part 820, and related quality system requirements.
Experience with CAPA, NCRs, MRBs, SCARs, SOPs, and audit preparation.
Excellent documentation, communication, and organizational skills.
Proficient with Microsoft Office; experience with electronic QMS software preferred.
Preferred Qualifications
Experience in injection molding, precision manufacturing, or medical device production.
Experience in Medical Device (ISO 13485) manufacturing industry.
Knowledge of ISO 9001/134855/FDA requirements and compliance.
Familiarity with GD&T, metrology equipment (CMM, optical systems), and statistical analysis tools (Minitab/Excel).
Ability to speak with customers.
Strong problem‑solving and cross‑functional teamwork abilities.
Language Ability
Ability to read, write, understand and follow instructions in the English language.
Effective oral and written communication in the English language.
Spanish is a plus.
Benefits: Medical; Dental; Vision; Life; STD; LTD; 401(k) with company match; Paid Time Off
Cinova Medical, Inc. is an Equal Opportunity Employer and a Drug Free Workplace.
Upon hire, Cinova Medical, Inc. uses E-Verify to verify employment eligibility for roles based in the United States.
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