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Quality Systems & Training Specialist

Santa Rosa, CA · On-site

$30 - $38/hr

QUALITY SYSTEMS & TRAINING SPECIALIST Santa Rosa, CA | $30-$38/hr DOE Position Summary Responsible ... Manage CAPA and complaint processes from investigation through closure. * Track audit findings ...

Blount Fine Foods

Supplier Quality Specialists

Warren, RI · On-site

$65K - $74K/yr

The specialist will update and manage the department's trackers for raw material approvals and ... Review, assess, and approve supplier CAPA responses, ensuring corrective actions are sustainable ...

Nidec Motor

... CAPA execution Support onboarding of new quality specialists as needed Qualifications Education & Experience Bachelor's degree in Quality, Life Sciences, Engineering, Manufacturing, Business, or ...

Nidec Corporation

... CAPA execution Support onboarding of new quality specialists as needed Qualifications * Education & Experience Bachelor's degree in Quality, Life Sciences, Engineering, Manufacturing, Business, or ...

Aequor

Specialist Manufacturing

Thousand Oaks, CA · On-site

The Specialist Manufacturing is expected to own and execute under minor supervision all the processes related to deviations (minor and majors), Corrective and Preventive Actions (CAPAs), CAPA ...

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How much do capa specialists jobs pay per year?

As of Sep 11, 2026, the average yearly pay for capa specialists in the United States is $66,611.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,500.00 and $78,500.00 per year, depending on experience, location, and employer.

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Infographic showing various Capa Specialists job openings in the United States as of June 2026, with employment types broken down into 88% Full Time, and 12% Part Time. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $66,611 per year, or $32 per hour.

Senior Quality Assurance Specialist

Richland, WA

Symmetrio
See more jobs at Symmetrioexternal

$86K - $118K/yr

Full-time

Re-posted 21 days ago

Job description

Symmetrio is recruiting a Senior Quality Assurance Specialist for a growing medical device company in Richland, Washington.

This position will provide quality oversight across the design, manufacturing, testing, and release of regulated medical devices. The Senior Quality Assurance Specialist will manage nonconformance and CAPA activities, support internal and external audits, monitor quality performance indicators, and help strengthen the organization's quality management system.

Responsibilities
  • Serve as the primary quality contact for manufacturing-related nonconformance and CAPA activities.
  • Review investigations for appropriate problem statements, root-cause analysis, corrections, and corrective or preventive actions.
  • Maintain NC and CAPA records within the electronic quality management system.
  • Ensure compliance with FDA 21 CFR requirements, ISO 13485, MDSAP, and other applicable standards.
  • Track quality performance indicators and present findings to management and cross-functional stakeholders.
  • Develop and conduct internal process audits.
  • Support notified-body audits and FDA inspections as a quality subject-matter expert.
  • Review and approve validation protocols, calibration records, analytical reports, and equipment maintenance records.
  • Monitor process controls, supplier quality, and product conformity.
  • Develop and improve manufacturing quality and compliance processes.
  • Provide quality-system training and support to team members.
  • Lead the resolution of quality issues involving manufacturing, operations, and support teams.
  • Perform additional quality-related responsibilities as assigned.

Requirements

  • Bachelor's degree in life sciences, engineering, or a related field, or an equivalent combination of education and experience.
  • At least eight years of quality assurance experience.
  • Experience within the medical device or pharmaceutical industry.
  • Working knowledge of FDA 21 CFR requirements, ISO 13485, and MDSAP.
  • Good Manufacturing Practices certification.
  • Experience managing nonconformance investigations and CAPA processes.
  • Strong knowledge of quality systems, manufacturing controls, and regulatory compliance.
  • Experience supporting internal audits, regulatory inspections, or notified-body audits.
  • Strong root-cause analysis, problem-solving, and process-improvement skills.
  • Excellent documentation, organization, and attention to detail.
  • Ability to interpret standard operating procedures and work instructions.
  • Strong written and verbal communication skills.
  • Ability to work effectively with cross-functional teams and manage multiple deadlines.
  • Proficiency with Microsoft Outlook, Word, Excel, and PowerPoint.
  • Experience working in a radiologically controlled environment is preferred.
  • Ability to work a flexible schedule and travel as needed.
  • Ability to successfully complete required background and drug screenings.

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