Quality Assurance Specialist Jobs in Tennessee
Quality Assurance Specialist jobs in Tennessee are steadily active, with consistent demand from the state's manufacturing, healthcare, and automotive supply chain sectors at levels from entry-level inspector through senior QA manager. Nashville, Memphis, and Chattanooga lead hiring volume, anchored by large employers such as Nissan, HCA Healthcare, and FedEx, all of which maintain substantial Tennessee operations. The most in-demand specialties include medical device quality compliance, automotive process auditing, and ISO standards implementation. Find a role that fits below and apply directly.
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Showing 5 of 66+ Quality Assurance Specialist jobs
HOW WE GOT HERE
For more than 40 years, BioIVT has evolved from a specialized biospecimen provider into a global partner to life science and diagnostic organizations. Our growth has been shaped by a consistent focus on helping researchers access the high-quality biospecimens, primary cells, ADME-Tox products, and research services they need to advance discovery, development, and medical progress.
What has remained constant throughout that history is our mission: to enable smarter science and accelerate medical breakthroughs that enhance and extend lives. Every BioIVT team member contributes to that mission, whether supporting a donor center, laboratory, commercial team, or corporate function. For employees, this means joining a company where scientific quality, operational excellence, compliance, collaboration, and customer focus all come together to support work that matters.
Essential Responsibilities
- Provide quality leadership and guidance to Donor Center operations, promoting a culture of compliance, accountability, and continuous improvement.
- Lead implementation, maintenance, and improvement of the Quality Management System to support regulatory compliance and business objectives.
- Oversee quality metrics, trend analysis, risk assessments, and performance monitoring to identify improvement opportunities and mitigate compliance risks.
- Lead Quality Management Reviews for assigned sites and ensure effective evaluation of quality system performance, audit results, customer feedback, risks, and improvement initiatives.
- Serve as the primary quality lead for customer audits, regulatory inspections, and compliance readiness activities.
- Review and approve deviations, nonconformances, complaints, investigations, CAPAs, and change controls, ensuring timely closure and effectiveness.
- Facilitate root cause investigations using risk-based and structured problem-solving methodologies.
- Participate in and provide guidance to Deviation Review Boards, Change Control Review Boards, Material Review Boards, and Quality Review Boards.
- Develop, review, and maintain SOPs and quality procedures to ensure standardized practices across Donor Centers.
- Oversee training program effectiveness and ensure personnel are qualified to perform assigned responsibilities.
- Support donor file review, product disposition, and release activities to ensure compliance with regulatory, quality, and customer requirements.
- Conduct internal audits, facility inspections, and quality system assessments to verify ongoing compliance and identify improvement opportunities.
- Review and approve equipment, process, computerized system validation, and qualification activities as assigned.
- Maintain QA records and documentation in accordance with record retention and archival requirements.
- Partner with clients, suppliers, and cross-functional stakeholders to provide quality and regulatory guidance that supports organizational goals.
Qualifications
- Strong knowledge of Quality Management Systems, GMP, GDP, quality risk management, and regulatory compliance.
- Experience leading investigations, CAPA programs, audits, inspections, and quality improvement initiatives.
- Knowledge of applicable FDA, state, and industry regulations governing donor center, laboratory, biologics, or tissue-related operations.
- Excellent leadership, communication, organizational, and problem-solving skills.
- Demonstrated ability to influence cross-functional teams and drive compliance in a dynamic operational environment.
Work Environment & Travel
Hybrid Position
- Employee must maintain a dedicated home workspace and reliable internet connection when working remotely.
- Expected onsite presence of at least three (3) days per week.
- Travel to donor centers and other company locations approximately once per month or as business needs require.
ALSO TRUE OF THE RIGHT PERSON
- You are mission-driven and take pride in contributing to work that helps advance science, medical progress, and better outcomes.
- You value collaboration and build trusted relationships by being respectful, responsive, and solutions-oriented.
- You bring a strong sense of ownership and accountability, following through on commitments and taking pride in the quality of your work.
- You are comfortable working in a fast-paced, growing organization where priorities can shift and good judgment, flexibility, and communication matter.
- You care about doing things the right way, with consistency, integrity, attention to detail, and respect for quality and compliance.
- You are curious, open to feedback, and committed to continuous improvement in how we work, learn, and grow together.
WHAT WE OFFER
- Comprehensive medical coverage with PPO/HRA and HDHP/HSA plan options.
- Company-funded HRA or HSA contributions, depending on the medical plan elected.
- Prescription drug coverage, virtual care through MDLIVE, and preventive care
- Dental coverage through Cigna and vision coverage through VSP.
- Company-paid life, AD&D, short-term disability, and long-term disability coverage.
- Flexible spending account options, including healthcare, limited purpose, and dependent care FSAs.
- 401(k) retirement plan with employer Safe Harbor matching contributions.
- Tuition reimbursement to support continued learning, professional growth, and career development.
- Paid time off, company-paid holidays, employee assistance resources, travel assistance, and voluntary benefit options.
EQUAL OPPORTUNITY AND BELONGING
At BioIVT, our mission to enable smarter science and accelerate medical breakthroughs is strengthened by the people who bring that work to life. We are committed to building a workplace where employees are treated with fairness, respect, and dignity, and where different experiences, perspectives, and ideas help us better serve our customers, partners, donors, and one another. BioIVT is proud to be an Equal Opportunity Employer and welcomes qualified applicants without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, disability, veteran status, genetic information, or any other status protected by applicable law. We are proud to be an Equal Opportunity Employer.
To Learn more about our mission and team culture, click here!
HOW WE GOT HERE
For more than 40 years, BioIVT has evolved from a specialized biospecimen provider into a global partner to life science and diagnostic organizations. Our growth has been shaped by a consistent focus on helping researchers access the high-quality biospecimens, primary cells, ADME-Tox products, and research services they need to advance discovery, development, and medical progress.
What has remained constant throughout that history is our mission: to enable smarter science and accelerate medical breakthroughs that enhance and extend lives. Every BioIVT team member contributes to that mission, whether supporting a donor center, laboratory, commercial team, or corporate function. For employees, this means joining a company where scientific quality, operational excellence, compliance, collaboration, and customer focus all come together to support work that matters.
Essential Responsibilities
- Provide quality leadership and guidance to Donor Center operations, promoting a culture of compliance, accountability, and continuous improvement.
- Lead implementation, maintenance, and improvement of the Quality Management System to support regulatory compliance and business objectives.
- Oversee quality metrics, trend analysis, risk assessments, and performance monitoring to identify improvement opportunities and mitigate compliance risks.
- Lead Quality Management Reviews for assigned sites and ensure effective evaluation of quality system performance, audit results, customer feedback, risks, and improvement initiatives.
- Serve as the primary quality lead for customer audits, regulatory inspections, and compliance readiness activities.
- Review and approve deviations, nonconformances, complaints, investigations, CAPAs, and change controls, ensuring timely closure and effectiveness.
- Facilitate root cause investigations using risk-based and structured problem-solving methodologies.
- Participate in and provide guidance to Deviation Review Boards, Change Control Review Boards, Material Review Boards, and Quality Review Boards.
- Develop, review, and maintain SOPs and quality procedures to ensure standardized practices across Donor Centers.
- Oversee training program effectiveness and ensure personnel are qualified to perform assigned responsibilities.
- Support donor file review, product disposition, and release activities to ensure compliance with regulatory, quality, and customer requirements.
- Conduct internal audits, facility inspections, and quality system assessments to verify ongoing compliance and identify improvement opportunities.
- Review and approve equipment, process, computerized system validation, and qualification activities as assigned.
- Maintain QA records and documentation in accordance with record retention and archival requirements.
- Partner with clients, suppliers, and cross-functional stakeholders to provide quality and regulatory guidance that supports organizational goals.
Qualifications
- Strong knowledge of Quality Management Systems, GMP, GDP, quality risk management, and regulatory compliance.
- Experience leading investigations, CAPA programs, audits, inspections, and quality improvement initiatives.
- Knowledge of applicable FDA, state, and industry regulations governing donor center, laboratory, biologics, or tissue-related operations.
- Excellent leadership, communication, organizational, and problem-solving skills.
- Demonstrated ability to influence cross-functional teams and drive compliance in a dynamic operational environment.
Work Environment & Travel
Hybrid Position
- Employee must maintain a dedicated home workspace and reliable internet connection when working remotely.
- Expected onsite presence of at least three (3) days per week.
- Travel to donor centers and other company locations approximately once per month or as business needs require.
ALSO TRUE OF THE RIGHT PERSON
- You are mission-driven and take pride in contributing to work that helps advance science, medical progress, and better outcomes.
- You value collaboration and build trusted relationships by being respectful, responsive, and solutions-oriented.
- You bring a strong sense of ownership and accountability, following through on commitments and taking pride in the quality of your work.
- You are comfortable working in a fast-paced, growing organization where priorities can shift and good judgment, flexibility, and communication matter.
- You care about doing things the right way, with consistency, integrity, attention to detail, and respect for quality and compliance.
- You are curious, open to feedback, and committed to continuous improvement in how we work, learn, and grow together.
WHAT WE OFFER
- Comprehensive medical coverage with PPO/HRA and HDHP/HSA plan options.
- Company-funded HRA or HSA contributions, depending on the medical plan elected.
- Prescription drug coverage, virtual care through MDLIVE, and preventive care
- Dental coverage through Cigna and vision coverage through VSP.
- Company-paid life, AD&D, short-term disability, and long-term disability coverage.
- Flexible spending account options, including healthcare, limited purpose, and dependent care FSAs.
- 401(k) retirement plan with employer Safe Harbor matching contributions.
- Tuition reimbursement to support continued learning, professional growth, and career development.
- Paid time off, company-paid holidays, employee assistance resources, travel assistance, and voluntary benefit options.
EQUAL OPPORTUNITY AND BELONGING
At BioIVT, our mission to enable smarter science and accelerate medical breakthroughs is strengthened by the people who bring that work to life. We are committed to building a workplace where employees are treated with fairness, respect, and dignity, and where different experiences, perspectives, and ideas help us better serve our customers, partners, donors, and one another. BioIVT is proud to be an Equal Opportunity Employer and welcomes qualified applicants without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, disability, veteran status, genetic information, or any other status protected by applicable law. We are proud to be an Equal Opportunity Employer.
To Learn more about our mission and team culture, click here!
See All 66 Quality Assurance Specialist Jobs in Tennessee
Find roles in Tennessee that match your experience and apply in just a few clicks.
Find JobsQuality Assurance Specialist Jobs by City in Tennessee
Where Tennessee roles are concentrated, by current openings.
Quality Assurance Specialist Job Market in Tennessee
A snapshot from current Tennessee openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals
- Manufacturing
- Food & Beverage
- Chemicals & Materials
- Healthcare & Medical Services
What Tennessee Employers Look For
The qualifications that appear most often in quality assurance specialist jobs across Tennessee.
- Bachelor's degree in a science, engineering, or technical field strongly preferred by Tennessee employers
- Familiarity with ISO 9001 or IATF 16949 quality management standards commonly required
- Experience using statistical process control methods and quality management software
- Proficiency with inspection tools, measurement systems analysis, and root cause analysis techniques
- Strong documentation skills and ability to write nonconformance reports and corrective action plans
- ASQ Certified Quality Auditor or Certified Quality Engineer credential recognized as a competitive advantage
Quality Assurance Specialist Jobs in Tennessee: Frequently Asked Questions
How do you become a quality assurance specialist in Tennessee?
Most Tennessee employers hire quality assurance specialists who hold a bachelor's degree in engineering, life sciences, manufacturing technology, or a related field, though an associate degree combined with hands-on industry experience is accepted in many manufacturing and logistics roles. Tennessee does not issue a state-specific license for QA specialists, but earning an ASQ certification such as the Certified Quality Technician or Certified Quality Inspector significantly strengthens candidacy, particularly for roles in automotive, medical device, and food manufacturing facilities.
Which companies hire quality assurance specialists in Tennessee?
Employers hiring quality assurance specialists in Tennessee right now include Food Lion, AAON, and Morgan Olson, based on current listings on Migrate Mate as of November 2026. Tennessee's concentration of automotive assembly plants, healthcare systems, and distribution centers means QA roles appear across a wide range of industries rather than clustering in a single sector.
Which Tennessee cities have the most quality assurance specialist jobs?
Memphis, Nashville, and Chattanooga account for the largest share of quality assurance specialist openings in Tennessee. Nashville's large healthcare and corporate headquarters presence drives demand there, while Memphis benefits from major logistics and food manufacturing operations, and Chattanooga's automotive corridor, anchored by Volkswagen and its supplier network, sustains strong demand for process and compliance-focused QA roles.
Are there remote quality assurance specialist jobs in Tennessee?
Yes, but they're limited, because quality assurance work often requires hands-on inspection, floor audits, and on-site supplier visits. About 24% of quality assurance specialist openings tied to Tennessee are remote or hybrid as of November 2026, which skews toward desk-based functions. The parts of the role most compatible with remote work are documentation review, supplier audit reporting, and quality management system administration.
How can I get hired as a quality assurance specialist in Tennessee with little or no experience?
The most realistic entry path is applying for quality technician or quality inspector roles, which Tennessee manufacturers and healthcare suppliers routinely fill with candidates who have an associate degree or relevant coursework rather than years of QA experience. Large Tennessee employers such as Nissan's Smyrna plant and Amazon's distribution network run structured onboarding programs for new inspectors. Earning an ASQ Certified Quality Technician credential before applying, or transitioning from a production operator or lab technician role, gives candidates without formal QA experience a concrete edge.
Where can I find and apply to quality assurance specialist jobs in Tennessee?
You can find and apply to quality assurance specialist jobs in Tennessee on Migrate Mate, which lists current openings from employers actively hiring in the state. Search the listings, find roles that match your experience and location, and apply directly to the ones that fit.
See All 66 Quality Assurance Specialist Jobs in Tennessee
Find roles in Tennessee that match your experience and apply in just a few clicks.
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