Senior Quality Engineer

Biolink360; Denver (CO); On-site; USD 95,000 - 140,000; Full time

Job summary

An established industry player is seeking a Senior Quality Engineer to enhance the quality assurance processes for SaMD applications. This pivotal role involves ensuring the reliability and functionality of software through rigorous testing and compliance with industry standards. The ideal candidate will lead efforts in continuous improvement, collaborating with cross-functional teams to drive quality initiatives. If you are passionate about quality engineering and eager to contribute to innovative healthcare solutions, this opportunity offers a dynamic environment to make a significant impact.

Qualifications

• 5+ Jahre Erfahrung in der Qualitätssicherung, insbesondere mit SaMD-Produkten.
• Kenntnisse in ISO 13485 und QMS sind erforderlich.

Responsibilities

• Implementierung von Qualitätsstandards und -verfahren für Softwareprodukte.
• Durchführung von Risikomanagement- und Designkontrollaktivitäten.

Skills

Qualitätsmanagementsysteme (QMS)

ISO 13485

IEC 62304

Risikomanagement

Software-Testmethoden

Education

BS oder MS in Ingenieurwissenschaften

Job description

Position: Senior Quality Engineer, SaMD
Location: Denver, CO
Reports to: Division VP
Salary Range: 95-140K

This company is leading the next evolution of clinical decision-making and patient workflow. We are seeking an experienced Quality Engineer to lead quality engineering activities. The person in this role will be responsible for ensuring the quality, functionality, and reliability of our SaMD applications through rigorous testing, analysis, and the implementation of quality assurance processes. This role is instrumental to drive continuous improvement efforts through facilitating, leading, and collaborating with cross function teams including quality, engineering, production, clinical, and regulatory affairs.

Responsibilities

• Assist in the implementation, compliance, and maintenance of standards (e.g., FDA, ISO13485) and Quality policies and procedures.
• Perform investigation of product nonconformance/complaints, root cause analysis, monitoring/trending of process and product, and escalation of identified issues
• Devise & implement quality standards for software quality processes, systems, and procedures to support the software life cycle.
• Perform design control and risk management activities by working closely with cross functional teams.
• Ensure product requirements for traceability, risk remediation and testability are met.
• Meet verification and validation deliverables for compliance with regulatory affairs requirements.
• Oversee gap analysis and remediation activities.

Qualifications

• BS or MS/Engineering Degree with 5+ years of experience,
• Previous experience working with Quality Management Systems (QMS), with knowledge of ISO 13485 and 21 CFR 820.
• Experience with IEC 62304.
• 2+ years of experience with SaMD products, preferably in the life science industry.
• DHF and Risk Management experience, to include reporting and remediation