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Senior Quality Engineer Medical Device Jobs in Reno, NV

hyve solutions

Sr. Quality Engineer

Carson City, NV · On-site

$86K - $117K/yr

The Senior Quality Engineer provides advanced quality engineering leadership within a PCBA manufacturing environment. This role leads complex investigations, systemic corrective actions, customer ...

Hyve Solutions

Sr. Quality Engineer

Carson City, NV · On-site

$86K - $117K/yr

The Senior Quality Engineer provides advanced quality engineering leadership within a PCBA manufacturing environment. This role leads complex investigations, systemic corrective actions, customer ...

Hamilton Medical, Inc.

Quality Engineer

Reno, NV · On-site

$75K - $85K/yr

Support in Medical Device reporting (MDRs), complaints, field corrective action (Recall) and management review meeting * Effectively engage in project as the Quality Engineering resource.

Hamilton Medical, Inc.

Quality Engineer

Reno, NV · On-site

$71K - $92K/yr

Support in Medical Device reporting (MDRs), complaints, field corrective action (Recall) and management review meeting * Effectively engage in project as the Quality Engineering resource.

Panasonic

Sr. Quality Lab Engineer

Sparks, NV · On-site

$90K - $122K/yr

Responsibilities Sr. Quality Lab Engineer (by clicking this link you are being referred to an ... Health Benefits - Offering medical, dental, vision, prescription plans, plus Health Savings Account ...

Timken

Senior Manufacturing Quality Engineer

Carson City, NV · On-site

$86K - $117K/yr

... medical and robotics innovation. From precision gears used in life-saving surgical robots to ... The Senior Manufacturing Quality Engineer (MQE) is responsible for investigating, managing analysis ...

Timken

Senior Manufacturing Quality Engineer

Carson City, NV · On-site

$86K - $117K/yr

... medical and robotics innovation. From precision gears used in life-saving surgical robots to ... The Senior Manufacturing Quality Engineer (MQE) is responsible for investigating, managing analysis ...

Timken

Quality Engineer

Carson City, NV · On-site

$70K - $91K/yr

Works with the Director of Manufacturing Systems, Manufacturing Engineering Manager or Senior ... ISO 13485 Medical Devices Quality Management and AS/EN 9100 Aerospace Quality Management Systems.

The Timken Company

Quality Engineer

Carson City, NV · On-site

$70K - $91K/yr

Works with the Director of Manufacturing Systems, Manufacturing Engineering Manager or Senior ... ISO 13485 Medical Devices Quality Management and AS/EN 9100 Aerospace Quality Management Systems.

Timken

Quality Engineer

Carson City, NV · On-site

$70K - $91K/yr

Works with the Director of Manufacturing Systems, Manufacturing Engineering Manager or Senior ... ISO 13485 Medical Devices Quality Management and AS/EN 9100 Aerospace Quality Management Systems.

The Timken Company

Quality Engineer

Carson City, NV · On-site

$70K - $91K/yr

Works with the Director of Manufacturing Systems, Manufacturing Engineering Manager or Senior ... ISO 13485 Medical Devices Quality Management and AS/EN 9100 Aerospace Quality Management Systems.

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All JobsQuality Engineer Medical Device JobsSenior Quality Engineer Medical Device JobsSenior Quality Engineer Medical Device Jobs in Reno, NV

Senior Quality Engineer Medical Device information

See Reno, NV salary details

$60.3K

$105K

$146.1K

How much do senior quality engineer medical device jobs pay per year?

As of Sep 9, 2026, the average yearly pay for senior quality engineer medical device in Reno, NV is $104,984.00, according to ZipRecruiter salary data. Most workers in this role earn between $88,200.00 and $119,600.00 per year, depending on experience, location, and employer.

What is a senior quality engineer medical device?

Senior Quality Engineers in the medical device industry are professionals responsible for ensuring that medical devices meet regulatory standards and quality requirements throughout their lifecycle. They lead quality assurance activities, develop and implement testing protocols, coordinate with design and manufacturing teams, and help ensure compliance with relevant regulations such as FDA and ISO standards. Their expertise ensures that products are safe, effective, and reliable for patient use. They also mentor junior engineers and may play a key role in audits and process improvements.

How does a senior quality engineer medical device typically collaborate with cross-functional teams during product development?

As a Senior Quality Engineer in the medical device sector, you will work closely with cross-functional teams including R&D, manufacturing, regulatory affairs, and supply chain. Your role involves ensuring quality standards are integrated throughout the product lifecycle, from design reviews and risk assessments to process validation and compliance documentation. Regular meetings, joint problem-solving sessions, and clear communication are vital to resolve issues efficiently and maintain regulatory compliance. This collaborative environment helps to ensure both product safety and timely market release.

What are the key skills and qualifications needed to thrive as a senior quality engineer medical device, and why are they important?

To excel as a Senior Quality Engineer in Medical Devices, you need a solid background in engineering, quality assurance, and regulatory compliance, typically with a relevant degree and experience in the medical device industry. Familiarity with ISO 13485, FDA 21 CFR Part 820, risk management tools (such as FMEA), and quality management systems is crucial, and certifications like CQE or Six Sigma are often preferred. Strong problem-solving, attention to detail, and effective communication skills distinguish top performers in this role. These competencies ensure product safety, regulatory compliance, and the continuous improvement of processes critical to patient outcomes and company success.

What is the difference between Senior Quality Engineer Medical Device vs Quality Engineer Medical Device?

AspectSenior Quality Engineer Medical DeviceQuality Engineer Medical Device
ResponsibilitiesLead quality initiatives, oversee audits, mentor team membersAssist in quality processes, support audits, perform inspections
Experience & CertificationsTypically 5+ years, often ISO 13485, FDA regulationsEntry to mid-level, basic knowledge of industry standards
Work EnvironmentLeadership roles, cross-functional teams, strategic planningOperational tasks, documentation, compliance support
Usage & IndustryCommonly used in manufacturing, R&D, and quality departmentsUsed across similar settings, often as a stepping stone role

The main difference between a Senior Quality Engineer Medical Device and a Quality Engineer Medical Device lies in experience, responsibilities, and leadership scope. Senior roles involve strategic oversight and mentorship, while standard Quality Engineers focus on supporting quality processes and compliance tasks.

What are popular job titles related to Senior Quality Engineer Medical Device jobs in Reno, NV?

For Senior Quality Engineer Medical Device jobs in Reno, NV, the most frequently searched job titles are:

What job categories do people searching Senior Quality Engineer Medical Device jobs in Reno, NV look for?

The top searched job categories for Senior Quality Engineer Medical Device jobs in Reno, NV are:

Senior Quality Engineer Medical Device jobs near you
Infographic showing various Senior Quality Engineer Medical Device job openings in Reno, NV as of September 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, 5% Contract, and 1% Nights. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $104,984 per year, or $50.5 per hour.

Sr. Quality Engineer

Carson City, NV • On-site

hyve solutions
Manufacturing • 1 - 5K employees
Learn more about hyve solutionsexternal

$86K - $117K/yr

Full-time

Re-posted 22 days ago

Hyve Solutions rating

6.1

Company rating: 6.1 out of 10

Based on 16 frontline employees who took The Breakroom Quiz

148th of 162 rated electronics manufacturers

Job description

@HYVE Solutions, missions to help customers, business partners, and employees achieve success through shared goals, strategies, resources and technology solutions.
The Senior Quality Engineer provides advanced quality engineering leadership within a PCBA manufacturing environment. This role leads complex investigations, systemic corrective actions, customer requirement translation, manufacturing process quality improvement, audit readiness support, and Quality Engineer mentorship. The Senior Quality Engineer serves as a systems-level quality leader and technical resource for Quality, Manufacturing, Engineering, Materials, Program Management, customers, and site leadership.
Key Responsibilities
  • Lead complex quality investigations involving customer escapes, recurring defects, systemic process failures, audit findings, and major nonconformances.
  • Drive containment, root cause analysis, corrective action, preventive action, effectiveness verification, and sustainment for significant quality issues.
  • Own the review, interpretation, communication, and implementation strategy for customer-specific quality requirements.
  • Translate customer requirements into operational controls across manufacturing, inspection, documentation, labeling, traceability, training, and quality records.
  • Identify gaps between customer requirements and site execution and drive cross-functional closure before they result in defects, escapes, or audit findings.
  • Provide technical quality engineering support for manufacturing processes, inspection criteria, process controls, corrective action strategy, and systemic risk reduction.
  • Mentor QE I and QE II team members in investigations, customer requirement interpretation, data analysis, process control, and corrective action discipline.
  • Support internal audits, process audits, customer audits, registrar audits, compliance assessments, management review inputs, and quality improvement planning.
  • Lead improvement projects tied to FPY, DPPM, scrap, rework, fallout, cost of poor quality, customer escapes, and audit readiness.
  • Perform other duties as assigned in support of Quality department objectives, customer requirements, production support, and QMS/EMS compliance.

Qualifications
  • Bachelor's degree in Engineering, Quality, Manufacturing, or related technical field preferred.
  • 5+ years of Quality Engineering experience in manufacturing.
  • 3+ years of electronics, PCBA, or related technical manufacturing experience preferred.
  • Strong knowledge of ISO 9001, corrective action systems, manufacturing process controls, and customer requirement implementation.
  • Experience with IPC-A-610, ISO 14001, SMT, AOI, AXI, inspection, test, and rework processes preferred.
  • Strong communication, technical judgment, cross-functional influence, and problem-solving skills.

Relocation assistance may be provided for this role based on candidate qualifications, location, and business needs.
@ HYVE Solutions, we believe employees are our greatest asset and we empower them to make a difference in our business. Diversity and inclusion make us all better. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability or protected veteran status.

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