Quality Specialist Jobs in Nevada
Quality Specialist jobs in Nevada are concentrated in Las Vegas, Reno, and Henderson, where manufacturing, gaming technology, and healthcare drive steady demand for professionals who specialize in process improvement, compliance auditing, and product quality assurance. Major employers with an established Nevada presence include Caesars Entertainment, Switch, and Renown Health, hiring quality specialists at levels from entry-level inspectors to senior quality engineers. Demand is particularly strong in regulated industries where documentation, corrective action, and ISO or FDA compliance expertise are required. Find a role that fits below and apply directly.
Find Quality Specialist JobsOverview
Showing 5 of 10+ Quality Specialist jobs
General Summary
The Junior Quality Specialist plans, coordinates, monitors and performs Quality System functions pertaining to Quality Control, Quality Improvement, Environmental Monitoring, Calibration, and Preventive Maintenance while ensuring that Origin Biologics maintains compliance to all regulatory requirements.
Functional Responsibilities
- Ability to support Good Manufacturing Practices (GMP), Good Tissue Practices (GTP) as well as manufacturing and distribution of Class II medical devices and allograft derived products
- Create Standard Operating Procedures, Work Instructions and any other documentation required to ensure compliance with current quality control requirements.
- Participates in the creation, management, scheduling and performance of the environmental monitoring program.
- Liaise with management teams to ensure ongoing development required to maintain efficient work practices within the facility.
- Assist in the development and implementation of continuous process improvements.
- Assist in the implementation of systems to ensure continued company compliance with all relevant regulations and standards set forth by regulatory, quality and/or accrediting agencies (required FDA 21 CFR 1271 and 21 CFR 820, AATB, and ISO 13485).
- Communicates Quality Control activities to management. Coordinates the design, collection and monitoring of metrics for reporting to departmental management for Quality Control.
- Facilitates internal assessments and audits, to assess the effectiveness of process improvement initiatives and to report to upper management regarding the status current Good Manufacturing Practices.
- Participates in the creation, management, scheduling and performance of the equipment preventative maintenance and calibration (PM/CAL) program.
- Performs tasks related to the general administration of the company’s Quality System, including but not limited to; creation, management and timely closure of Out-of-Specification results, Non-Conformances, CAPAs and Change Controls.
- Maintains a current working knowledge of all relevant laws, regulations and industry applicable standards (GMP, GTP, ISO 13485, FDA 21 CFR 1271, AATB and 21 CFR 820).
- Assists in the creation, management, scheduling and performing of GMP, GTP and competency training for staff.
- Assist with the preparation of monthly quality metrics and system trending for reporting.
- Performs other duties as required or assigned.
- Conduct audits (internal/supplier) to assess compliance to regulations, standards, and procedures.
Non-Functional Responsibilities:
- Ability to promote the organization, its vision and reinforce brand awareness and visibility
- Represent the organization at events, functions, society and conference meetings
- Ability to provide agile, creative solutions to expedite go-to-market strategies
- Ability to Interact with internal and external customers to ensure the best possible QA/RA customer experience
Culture:
- Dynamic, fast paced start-up environment
- Relentless focus on execution, accountability, quality and delivery schedule
- Apply agile and creative solutions to build disruptive business model
Job Qualifications:
- Education: B.A/B.Sc. in physical, applied and/or life sciences, engineering or mathematics is required with five (5) years of relevant experience; or at least two (2) years of relevant experience.
Experience:
- At least two (2) years of experience in a regulated industry experience or with related products (Medical Devices, biologics or allograft). Experience with American Association of Tissue Banks (AATB) and International agencies (Australia, Asia, South and Central America and Mexico) and European Medicines Agency (EMA) is preferred.
Certifications/Licenses:
- Certificates from accredited programs, American Society for Quality (ASQ) Certified Quality Auditor (CQA), Regulatory Affairs Certificate (RAC), Certified Tissue Bank Specialist (CTBS) are strongly recommended.
Other:
- Knowledge of Quality terms, tools and methodologies. Good mathematical and computer skills including competence in Microsoft Office required. Work requires the mental ability and skills necessary to conform to the standards of the procedure manual, FDA regulations, AATB standards, ISO standard, OSHA requirements and all other relative requirements.
Job Type: Full-time
Pay: $20.00 - $24.00 per hour
Benefits:
- 401(k)
- Dental insurance
- Employee assistance program
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
Work Location: In person
General Summary
The Junior Quality Specialist plans, coordinates, monitors and performs Quality System functions pertaining to Quality Control, Quality Improvement, Environmental Monitoring, Calibration, and Preventive Maintenance while ensuring that Origin Biologics maintains compliance to all regulatory requirements.
Functional Responsibilities
- Ability to support Good Manufacturing Practices (GMP), Good Tissue Practices (GTP) as well as manufacturing and distribution of Class II medical devices and allograft derived products
- Create Standard Operating Procedures, Work Instructions and any other documentation required to ensure compliance with current quality control requirements.
- Participates in the creation, management, scheduling and performance of the environmental monitoring program.
- Liaise with management teams to ensure ongoing development required to maintain efficient work practices within the facility.
- Assist in the development and implementation of continuous process improvements.
- Assist in the implementation of systems to ensure continued company compliance with all relevant regulations and standards set forth by regulatory, quality and/or accrediting agencies (required FDA 21 CFR 1271 and 21 CFR 820, AATB, and ISO 13485).
- Communicates Quality Control activities to management. Coordinates the design, collection and monitoring of metrics for reporting to departmental management for Quality Control.
- Facilitates internal assessments and audits, to assess the effectiveness of process improvement initiatives and to report to upper management regarding the status current Good Manufacturing Practices.
- Participates in the creation, management, scheduling and performance of the equipment preventative maintenance and calibration (PM/CAL) program.
- Performs tasks related to the general administration of the company’s Quality System, including but not limited to; creation, management and timely closure of Out-of-Specification results, Non-Conformances, CAPAs and Change Controls.
- Maintains a current working knowledge of all relevant laws, regulations and industry applicable standards (GMP, GTP, ISO 13485, FDA 21 CFR 1271, AATB and 21 CFR 820).
- Assists in the creation, management, scheduling and performing of GMP, GTP and competency training for staff.
- Assist with the preparation of monthly quality metrics and system trending for reporting.
- Performs other duties as required or assigned.
- Conduct audits (internal/supplier) to assess compliance to regulations, standards, and procedures.
Non-Functional Responsibilities:
- Ability to promote the organization, its vision and reinforce brand awareness and visibility
- Represent the organization at events, functions, society and conference meetings
- Ability to provide agile, creative solutions to expedite go-to-market strategies
- Ability to Interact with internal and external customers to ensure the best possible QA/RA customer experience
Culture:
- Dynamic, fast paced start-up environment
- Relentless focus on execution, accountability, quality and delivery schedule
- Apply agile and creative solutions to build disruptive business model
Job Qualifications:
- Education: B.A/B.Sc. in physical, applied and/or life sciences, engineering or mathematics is required with five (5) years of relevant experience; or at least two (2) years of relevant experience.
Experience:
- At least two (2) years of experience in a regulated industry experience or with related products (Medical Devices, biologics or allograft). Experience with American Association of Tissue Banks (AATB) and International agencies (Australia, Asia, South and Central America and Mexico) and European Medicines Agency (EMA) is preferred.
Certifications/Licenses:
- Certificates from accredited programs, American Society for Quality (ASQ) Certified Quality Auditor (CQA), Regulatory Affairs Certificate (RAC), Certified Tissue Bank Specialist (CTBS) are strongly recommended.
Other:
- Knowledge of Quality terms, tools and methodologies. Good mathematical and computer skills including competence in Microsoft Office required. Work requires the mental ability and skills necessary to conform to the standards of the procedure manual, FDA regulations, AATB standards, ISO standard, OSHA requirements and all other relative requirements.
Job Type: Full-time
Pay: $20.00 - $24.00 per hour
Benefits:
- 401(k)
- Dental insurance
- Employee assistance program
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
Work Location: In person
See All 10 Quality Specialist Jobs in Nevada
Find roles in Nevada that match your experience and apply in just a few clicks.
Find Quality Specialist JobsQuality Specialist Jobs by City in Nevada
Where Nevada roles are concentrated, by current openings.
Quality Specialist Job Market in Nevada
A snapshot from current Nevada openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Healthcare & Medical Services
What Nevada Employers Look For
The qualifications that appear most often in quality specialist jobs across Nevada.
- Bachelor's degree in engineering, life sciences, or a related technical field
- Hands-on experience with ISO 9001, FDA, or industry-specific quality management systems
- Certified Quality Auditor (CQA) or Certified Quality Engineer (CQE) credential from ASQ
- Proficiency in root cause analysis, corrective and preventive action processes
- Experience with statistical process control tools and quality data documentation
- Strong written communication skills for audit reports and regulatory submissions
Quality Specialist Jobs in Nevada: Frequently Asked Questions
How do you become a quality specialist in Nevada?
Most quality specialist roles in Nevada require a bachelor's degree in engineering, manufacturing, life sciences, or a related field, combined with practical quality management experience. Nevada does not issue a state-specific license for quality specialists, but employers in regulated sectors such as healthcare and medical device manufacturing expect nationally recognized credentials like the ASQ Certified Quality Engineer or Certified Quality Auditor. Building experience in ISO or FDA-regulated environments significantly strengthens a candidate's profile.
Which companies hire quality specialists in Nevada?
Employers hiring quality specialists in Nevada right now include Planet 13, CSL Plasma, and SOLV Energy, based on current listings on Migrate Mate as of November 2026. Nevada's concentration of data center operators, healthcare systems, and light manufacturing facilities creates consistent demand for quality professionals with compliance and process improvement backgrounds.
Which Nevada cities have the most quality specialist jobs?
Las Vegas, Reno, and Yerington account for the largest share of quality specialist openings in Nevada. Las Vegas leads because of its scale as the state's largest metro, with concentrated activity in healthcare, gaming technology, and distribution, while Reno and Henderson attract roles tied to manufacturing operations and the growing industrial corridor along Interstate 80.
Are there remote quality specialist jobs in Nevada?
Yes, but they're rare. Quality specialist work is largely hands-on, involving physical inspections, audits of production lines, and on-site regulatory reviews that require an in-person presence. About 25% of quality specialist openings tied to Nevada are remote or hybrid as of November 2026, and those positions tend to be documentation-heavy or system-audit roles where physical presence is not required on a daily basis.
How can I get hired as a quality specialist in Nevada with little or no experience?
The most realistic entry path is a quality technician or quality inspector role at a Nevada manufacturer or healthcare supplier, where on-the-job exposure to audits and documentation provides a foundation. Large employers in the Las Vegas and Reno corridors, including distribution centers and medical device suppliers, regularly hire associates from adjacent roles such as production supervisor, lab technician, or compliance coordinator. Pursuing an ASQ entry-level certification or completing coursework in quality management systems gives candidates a measurable edge in a competitive applicant pool.
Where can I find and apply to quality specialist jobs in Nevada?
You can find and apply to quality specialist jobs in Nevada on Migrate Mate, which lists current openings across the state. Search the roles available, find the ones that match your experience and location, and apply directly to the employers posting them.
See All 10 Quality Specialist Jobs in Nevada
Find roles in Nevada that match your experience and apply in just a few clicks.
Find Quality Specialist Jobs