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Laboratory Quality Jobs (NOW HIRING)

Tanaq

Laboratory Quality Specialist III

Atlanta, GA · On-site

The Laboratory Quality Specialist III will develop, monitor, and maintain the quality management system for our client. This is a hybrid remote position that will require some onsite work in Atlanta ...

HaysMed

Laboratory Quality Coordinator

Hays, KS · On-site

Under direction of the Director of Laboratory Operations, the Laboratory Quality Coordinator supports the Quality Management System (QMS) for all Clinical Pathology (CP) laboratory sections in ...

Tanaq

Laboratory Quality Specialist III

Atlanta, GA · On-site

The Laboratory Quality Specialist III will develop, monitor, and maintain the quality management system for our client. This is a hybrid remote position that will require some onsite work in Atlanta ...

HaysMed

Laboratory Quality Coordinator

Hays, KS · On-site

Under direction of the Director of Laboratory Operations, the Laboratory Quality Coordinator supports the Quality Management System (QMS) for all Clinical Pathology (CP) laboratory sections in ...

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Laboratory Quality information

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How much do laboratory quality jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for laboratory quality in the United States is $22.61, according to ZipRecruiter salary data. Most workers in this role earn between $18.99 and $24.04 per hour, depending on experience, location, and employer.

What is a laboratory quality professional?

A Laboratory Quality professional is responsible for ensuring that laboratory processes, procedures, and results comply with regulatory standards and quality management systems. They oversee quality assurance and quality control activities, conduct audits, implement corrective actions, and help maintain accreditation requirements. Their work ensures that laboratory data is accurate, reliable, and meets industry or governmental guidelines, which is critical for patient safety and research integrity.

What are some common challenges faced in a laboratory quality role, and how can they be addressed?

Professionals in Laboratory Quality roles often encounter challenges such as maintaining compliance with evolving regulatory standards, ensuring accurate documentation, and managing audits. Staying up to date with industry regulations and fostering ongoing communication with laboratory staff can help address these challenges. Additionally, implementing robust quality management systems and regular training programs can ensure consistency and preparedness for internal and external audits.

What are the key skills and qualifications needed to thrive in laboratory quality, and why are they important?

To excel in Laboratory Quality, strong knowledge of laboratory standards, regulatory compliance, and quality management systems is essential, often supported by a degree in a science field and experience with lab audits or certifications like ASQ or ISO 15189. Familiarity with Laboratory Information Management Systems (LIMS), proficiency in data analysis tools, and understanding of relevant accreditation processes are typically required. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for ensuring accuracy and driving continuous improvement. These competencies ensure laboratories produce reliable results, maintain regulatory compliance, and uphold safety and operational excellence.

What is the difference between Laboratory Quality vs Laboratory Technician?

AspectLaboratory QualityLaboratory Technician
CertificationsQuality certifications (e.g., ISO 17025)Technical certifications or training
Work EnvironmentQuality assurance departments, labs focusing on complianceLaboratory testing and analysis settings
Primary ResponsibilitiesDeveloping, implementing, and monitoring quality systemsPerforming tests, preparing samples, recording data
Industry UsageUsed across labs to ensure standards and complianceHands-on testing roles within labs

Laboratory Quality professionals focus on maintaining and improving lab standards through quality management systems, while Laboratory Technicians perform the actual testing and analysis. Both roles are essential but differ in responsibilities and focus areas within the laboratory environment.

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Laboratory Quality jobs near you
Infographic showing various Laboratory Quality job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $47,039 per year, or $22.6 per hour.

Laboratory Quality Specialist

STAQ Pharma Inc

Columbus, OH • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New

Job description

Job Summary:

The Laboratory Quality Specialist is responsible for maintaining and continuously improving the laboratory Quality Management System (QMS) in support of regulatory compliance, data integrity, product quality, laboratory impartiality, and patient safety within a regulated pharmaceutical laboratory environment. This role provides quality oversight for laboratory operations, testing support systems, documentation, investigations, audits, supplier and equipment quality activities, COA release, and inspection readiness.

This position works closely with the Laboratory Manager to support laboratory quality priorities, coordinate quality system activities, communicate compliance expectations, and help ensure laboratory operations remain aligned with regulatory requirements, internal procedures, continuous improvement goals, and the impartiality of the laboratory from manufacturing operations. The role requires strong knowledge of cGMP, GLP, applicable USP expectations, FDA-regulated laboratory practices, quality systems, risk management, and effective cross-functional collaboration.

Responsibilities: 

Quality Management System Support & Governance

  • Maintain and improve the laboratory QMS to ensure alignment with cGMP, GLP, applicable USP chapters, regulatory expectations, internal quality standards, and laboratory impartiality requirements.
  • Review and approve laboratory quality policies, SOPs, forms, logs, quality plans, and work instructions.
  • Maintain quality system processes for deviation management, CAPA, change control, risk management, document control, training, supplier qualification, audit readiness, management review, and objective quality decision-making independent from manufacturing pressure or conflicts of interest.
  • Define, monitor, trend, and report laboratory quality metrics to identify compliance risks, impartiality risks, recurring issues, and continuous improvement opportunities.
  • Partner with laboratory leadership and cross-functional stakeholders to ensure the QMS supports reliable testing, defensible data, timely investigations, compliant decisions, and quality system gap remediation.
  • Other duties as assigned.

Regulatory Compliance, Documentation, Data Integrity & Continuous Improvement

  • Oversee quality aspects of laboratory equipment qualification, calibration, maintenance, cleaning, environmental controls, temperature monitoring, and computerized or electronic laboratory systems.
  • Review and approve method implementation, transfer, verification, validation, and lifecycle maintenance from a quality and regulatory perspective.
  • Support regulatory inspections, client audits and internal audits.
  • Perform deviation investigations, CAPA, OOS/OOT investigations, change control, training qualifications, and COA review/release.
  • Review laboratory trends, deviations, complaints, audit findings, analytical report accuracy, and process performance to identify systemic issues and recommend preventive actions.
  • Contribute to monthly and quarterly quality metrics reporting, including trend analysis, risk escalation, and action tracking.
  • Lead or participate in continuous improvement projects that strengthen laboratory compliance, quality processes, efficiency, documentation, and operational reliability.
  • Support supplier assessment and qualification activities for laboratory materials, services, contract testing laboratories, calibration providers, and critical vendors.

Required Skills/Abilities: 

  • Strong working knowledge of GxP, including cGMP, GLP, FDA-regulated laboratory expectations, applicable USP requirements, and pharmaceutical quality systems.
  • Demonstrated ability to maintain and improve laboratory QMS, including document control, training, deviations, CAPA, change control, audits, supplier quality, management review, data integrity, and impartiality controls.
  • Excellent written and verbal communication skills, including technical writing, investigation documentation, root cause analysis, and client or auditor communication.
  • Ability to confidently interact with clients, auditors, laboratory staff, manufacturing partners, leadership, and internal stakeholders while supporting independent, objective quality decisions.
  • High attention to detail with strong judgment, integrity, confidentiality, and commitment to data integrity, patient safety, and laboratory impartiality.
  • Ability to interpret regulatory requirements and translate them into practical procedures, training, controls, and quality decisions.
  • Proficiency with Microsoft Office, including Excel, Word, and PowerPoint; experience with quality management systems, LIMS, electronic document management systems, and data trending tools preferred.

Education and Experience:

  • Bachelor’s degree in Chemistry, Biology, Biochemistry, Microbiology, Pharmaceutical Sciences, Medical Laboratory Science, or a related scientific discipline required; advanced degree preferred.
  • Minimum of 4 years of QA /QC experience within a pharmaceutical or regulated laboratory environment required.
  • Experience supporting regulatory inspections, client audits, internal audits, deviation investigations, CAPA, OOS/OOT investigations, change control, training systems, analytical report and COA review/release, and QMS implementation preferred.
  • ASQ, RAC, ISO 9001, ISO 17025, Lean Six Sigma, or related quality/regulatory certification preferred but not required.

Physical Requirements: 

  • Ability to stand for extended periods while performing laboratory procedures.
  • Ability to lift up to 25 lbs. (media, solvent containers, equipment parts).
  • Work performed in controlled laboratory environments.
  • Position may require occasional weekend, holiday, or off-shift work depending on laboratory needs.

Benefits:

  • Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options.
  • Life and disability insurance.
  • 401(k) with company match.
  • Paid vacation and holidays.