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Senior Quality Engineer

Job in Denver, Denver County, Colorado, 80285, USA
Listing for: Biolink360
Full Time position
Listed on 2026-02-06
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
  • Engineering
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 95000 - 140000 USD Yearly USD 95000.00 140000.00 YEAR
Job Description & How to Apply Below

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, ISO
13485) 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

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Position Requirements
10+ Years work experience
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