Quality Engineer in New York at Jobgether
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Job Description
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Quality Engineer based in the United States.
This role offers the opportunity to serve as a key quality engineering resource within a growing medical device organization. You will support the Quality Management System across product development, manufacturing, supplier operations, and post-market activities. Working closely with Engineering, Operations, Regulatory Affairs, and external suppliers, you will investigate issues and help drive effective, compliant solutions. The position combines hands-on problem solving with continuous improvement, risk management, and quality system oversight. You will contribute to CAPA, audits, supplier quality, change management, and regulatory readiness. This is an ideal opportunity for a quality professional who enjoys cross-functional collaboration and making a measurable impact on product quality and operational effectiveness.
- Investigate product, supplier, manufacturing, and quality system issues, supporting root cause analysis and effective resolution.
- Support CAPA activities from investigation and root cause analysis through action planning, implementation, effectiveness verification, and follow-up.
- Review design, material, supplier, process, engineering, and documentation changes and assess their potential quality and regulatory impact.
- Support risk management activities, including maintaining risk management files and evaluating changes that may affect product risk.
- Partner with Engineering, Operations, Regulatory Affairs, and suppliers to identify practical and compliant solutions to quality-related issues.
- Support supplier quality programs, including supplier issue investigations, corrective actions, change assessments, communications, and onboarding of new suppliers or contract manufacturers.
- Participate in internal audits and support external audits, regulatory inspections, and certification activities.
- Maintain and strengthen Quality Management System processes, including document control, training, quality metrics, audit readiness, and continuous improvement initiatives.
- Review quality records, change orders, engineering documentation, and other quality system records for accuracy, completeness, and compliance.
- Track quality actions and commitments to ensure they are completed, properly documented, and sustained.
- Serve as a technical quality resource to Engineering and other functional teams, providing guidance on quality system requirements, risk management, change control, investigations, and corrective actions.
- Identify opportunities to improve quality processes, operational effectiveness, and overall quality performance.
- Bachelor’s degree in Engineering, Quality, Life Sciences, or another related technical discipline.
- 5–8 years of experience in Quality Engineering, Quality Assurance, or Quality Systems within the medical device industry.
- Working knowledge of FDA Quality System Regulation, ISO 13485, risk management principles, and medical device quality requirements.
- Demonstrated experience supporting investigations, CAPA, supplier quality activities, and change management processes.
- Experience collaborating cross-functionally with Engineering, Manufacturing, Operations, Regulatory Affairs, and suppliers.
- Strong technical problem-solving, analytical, organizational, and communication skills.
- Ability to manage multiple projects and competing priorities effectively in a fast-paced environment.
- Strong interpersonal skills and the ability to communicate quality requirements and technical issues clearly to diverse stakeholders.
- Professional proficiency in English.
- Professional proficiency with Microsoft Office applications.
- Experience working with contract manufacturers and supplier quality programs is preferred.
- Experience participating in regulatory inspections and certification audits is preferred.
- ASQ Quality Engineer certification or an equivalent quality certification is a plus.
- Experience with electronic Quality Management Systems and Product Lifecycle Management systems is preferred, with Arena experience being an advantage.
- Base salary of $95,000–$105,000 annually.
- Comprehensive benefits package beginning on Day 1.
- Medical, dental, and vision insurance.
- Life insurance coverage.
- 401(k) plan with employer matching.
- Opportunity to contribute to quality, compliance, innovation, and continuous improvement within a medical device environment.
- Remote work arrangement.
- Equal opportunity workplace committed to diversity, inclusion, and accessibility.