Associate Quality Auditor
Listed on 2026-08-10
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Regulatory Compliance Specialist, Quality Engineering, Quality Control - QC Analysts/Managers
Associate Quality Auditor
Are you looking for an opportunity to make a difference? At Mesa Labs we're passionate about protecting the vulnerable by enabling scientific breakthroughs, ensuring product integrity, increasing patient and worker safety, and improving quality of life around the world.
At Mesa Labs we offer competitive wages, including bonus opportunity, and a comprehensive benefits package.
Base Compensation Range: $27.04 to $33.77 ph. This position is eligible for an annual 10% bonus opportunity in addition to the base salary.
Outstanding Benefits and Perks:
- Eligible for benefits the first day of the month after you start
- Tiered medical, dental and vision insurance options
- Health savings (HSA), healthcare & dependent care flexible spending (FSA) accounts
- Company paid short term and long-term disability (unless covered by a state disability plan)
- Company paid life insurance and AD&D
- 3 weeks of accrued vacation time; accruals begin on Day 1
- Paid sick leave of 48 hours per calendar year
- Eligible employees may receive four (4) weeks paid Care Giver leave after 1 year of service or in accordance with state leave laws
- 401(k) plan that provides a 4% Safe Harbor company match on a 4% employee contribution that begins on Day 1
- Employee Wellness and Financial Assistance Resources through Cigna and NY Life
- Nine (9) paid company holidays per year
- Overtime opportunities
SDC:
Sterilization and Disinfection Control division manufactures and sells biological and chemical indicators that assess the effectiveness of sterilization and disinfection processes for pharmaceutical, healthcare, and dental industries.
The Associate Quality Auditor plans, conducts, and reports on customer audits, internal quality audits and risk assessments across manufacturing, production, and process environments. This role ensures compliance with internal quality systems and applicable external regulations and standards, including GLP, GMP, ISO, and Six Sigma principles. Operating with supervision, the Associate Quality Auditor applies directed judgment to identify compliance gaps, assess risk, recommend corrective actions, and support continuous improvement initiatives.
Duties & Responsibilities:
Audit Planning & Execution
- Plan, schedule, and conduct internal quality audits of manufacturing, production, and process controls.
- Develop audit plans, checklists, and sampling strategies based on applicable standards, historical performance, and risk profiles.
- Execute audits to assess compliance with internal procedures and external regulations (e.g., GLP, GMP, ISO).
- Identify nonconformances, trends, and systemic risks affecting product quality or regulatory compliance.
Reporting & Follow-Up:
- Prepare clear, accurate, and well-structured written internal audit reports documenting observations, findings, and risk assessments.
- Communicate audit results to management and relevant stakeholders in a professional and constructive manner.
- Provide recommendations for corrective and preventive actions (CAPA) and support follow-up activities to verify effectiveness.
- Maintain audit documentation in accordance with quality system and record retention requirements.
External Audit Support:
- Support and/or facilitate external audits conducted by customers, registrars, or regulatory bodies, as needed.
- Serve as a point of contact during on-site audit activities, providing documentation, clarification, and coordination.
Quality Systems & Continuous Improvement:
- Contribute to the continuous improvement of audit processes, tools, and methodologies.
- Provide guidance to cross-functional teams on audit readiness, quality system expectations, and compliance best practices.
- Identify opportunities to reduce risk, improve controls, and strengthen overall quality system effectiveness.
Education & Experience:
- Bachelor's degree in Quality, Engineering, Life Sciences, or a related technical field required.
- 0-2 years of experience in quality assurance, quality auditing, or regulated manufacturing environments.
Knowledge, Skills & Abilities:
- Knowledge of quality systems and regulatory standards (GLP, GMP, ISO, Six Sigma concepts).
- Ability to plan and conduct audits with guidance and sound…
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