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Capa Jobs in Atlanta, GA (NOW HIRING)

SoftWave TRT

Quality Manager

Marietta, GA · On-site

This role will own the quality system framework, supplier quality oversight, CAPA administration, audit readiness, and regulatory support activities, while working cross-functionally with Operations ...

New

Abbott

Manager, Quality Assurance

Atlanta, GA · On-site

Lead site's CAPA program and drive continuous improvements by providing strategic direction for robust CAPA investigations and implementation of global resolutions while ensuring sustainability and ...

Deloitte

System Test and Validation Lead

Atlanta, GA · On-site +1

Lead CAPA activities for validation findings, including root cause analysis, effectiveness checks, closure documentation, and tracking of open compliance actions * Validate AI/ML-enabled GxP systems ...

Deloitte

System Test and Validation Lead

Atlanta, GA · On-site

Lead CAPA activities for validation findings, including root cause analysis, effectiveness checks, closure documentation, and tracking of open compliance actions * Validate AI/ML-enabled GxP systems ...

Abbott

Manager, Quality Assurance

Atlanta, GA

Lead site's CAPA program and drive continuous improvements by providing strategic direction for robust CAPA investigations and implementation of global resolutions while ensuring sustainability and ...

Deloitte

System Test and Validation Lead

Atlanta, GA · On-site

Lead CAPA activities for validation findings, including root cause analysis, effectiveness checks, closure documentation, and tracking of open compliance actions * Validate AI/ML-enabled GxP systems ...

Deloitte

System Test and Validation Lead

Atlanta, GA · On-site +1

Lead CAPA activities for validation findings, including root cause analysis, effectiveness checks, closure documentation, and tracking of open compliance actions * Validate AI/ML-enabled GxP systems ...

Abbott

Manager, Quality Assurance

Atlanta, GA · On-site

Lead site's CAPA program and drive continuous improvements by providing strategic direction for robust CAPA investigations and implementation of global resolutions while ensuring sustainability and ...

Deloitte

System Test and Validation Lead

Atlanta, GA · On-site +1

Lead CAPA activities for validation findings, including root cause analysis, effectiveness checks, closure documentation, and tracking of open compliance actions * Validate AI/ML-enabled GxP systems ...

Tanaq

Lab QMS Project Manager

Atlanta, GA · On-site

CAPA and Nonconformance Management: Track nonconforming events, feedback, complaints, root cause analyses, corrective actions, preventive actions, effectiveness checks, and trend reports to support ...

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How much do capa jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for capa in Atlanta, GA is $41.75, according to ZipRecruiter salary data. Most workers in this role earn between $31.65 and $48.55 per hour, depending on experience, location, and employer.

What are the typical daily responsibilities of a CAPA specialist?

A CAPA specialist is responsible for investigating quality issues, identifying root causes, and implementing corrective and preventive actions to ensure ongoing compliance and product integrity. Their typical day involves reviewing nonconformance reports, collaborating with cross-functional teams, documenting findings, and tracking the progress of CAPA initiatives using specialized software. CAPA specialists also prepare reports for audits and may facilitate meetings to drive continuous improvement activities. This role often requires balancing multiple projects and deadlines in a regulated environment, making organizational and communication skills crucial for success.

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

To thrive as a CAPA (Corrective and Preventive Action) specialist, you need expertise in quality management systems, root cause analysis, and compliance with industry standards, typically backed by a degree in engineering, life sciences, or a related field. Familiarity with CAPA software, regulatory frameworks (such as ISO 13485 or FDA 21 CFR Part 820), and document control systems is essential. Strong analytical thinking, attention to detail, and effective communication skills are vital soft skills for this role. These skills ensure effective problem-solving and sustained compliance, which are essential for maintaining product quality and meeting regulatory requirements.

What is a CAPA?

A CAPA (Corrective and Preventive Action) job involves identifying, investigating, and resolving quality issues in industries like manufacturing, healthcare, and pharmaceuticals. CAPA professionals analyze root causes of defects or process failures and implement corrective actions to prevent recurrence. They ensure compliance with regulatory standards, document findings, and improve overall quality management systems. Their role is critical in maintaining product safety, efficiency, and regulatory adherence.

What are the most commonly searched types of Capa jobs in Atlanta, GA? The most popular types of Capa jobs in Atlanta, GA are:
What are popular job titles related to Capa jobs in Atlanta, GA? For Capa jobs in Atlanta, GA, the most frequently searched job titles are:
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Capa jobs near you
Infographic showing various Capa job openings in Atlanta, GA as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $86,832 per year, or $41.7 per hour.

Quality Manager

SoftWave TRT

Marietta, GA • On-site

Full-time

Posted yesterday

New

Job description

Position Overview:
The Quality Manager will lead the company’s Quality Management System (QMS) and compliance infrastructure
to ensure ongoing adherence to applicable medical device quality and regulatory requirements, including ISO
13485 and FDA Quality System Regulations / QMSR.
This role will own the quality system framework, supplier quality oversight, CAPA administration, audit readiness,
and regulatory support activities, while working cross-functionally with Operations, Engineering, Regulatory
Affairs, and Service teams.
The Quality Manager will serve as the primary owner of the company’s quality system governance, ensuring that
processes, records, and corrective actions are maintained in a state of continuous compliance and audit readiness.
This role is critical to maintaining the company’s regulatory credibility, audit readiness, and quality system
integrity as SoftWave scales. The position ensures the company maintains a strong compliance backbone while enabling growth and operational execution.
Responsibilities:
Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.
Quality Management System (QMS) Ownership
  • Own and maintain the company’s QMS in alignment with applicable medical device standards
  • Develop, implement, and maintain procedures, SOPs, work instructions, and quality records
  • Manage document control, revision control, and training documentation processes
  • Ensure continuous audit readiness across all quality system elements
CAPA Ownership
  • Lead the Corrective and Preventive Action (CAPA) system
  • Ensure timely initiation, investigation, root cause analysis, and closure of CAPAs
  • Verify effectiveness of corrective actions
  • Drive cross-functional accountability for issue resolution and process improvement
Supplier Quality Oversight
  • Lead supplier qualification and quality oversight activities
  • Establish supplier quality agreements and quality performance metrics
  • Manage supplier corrective action requests (SCARs)
  • Conduct supplier quality reviews and support supplier audits
  • Partner with Supply Chain and Operations on supplier performance and issue resolution
Audit Leadership
  • Lead internal audit planning and execution
  • Serve as primary quality lead for external audits, customer audits, and certification audits
  • Coordinate responses to audit findings and corrective actions
  • Maintain audit schedules, records, and follow-up activities

Regulatory; Compliance Support
  • Support Regulatory Affairs with submission documentation and compliance records
  • Maintain quality documentation required for FDA and ISO compliance
  • Support inspection readiness and regulatory audit responses
  • Ensure quality system documentation supports product lifecycle and change control activities
    Change Control; Quality Records
  • Manage engineering change control and quality record processes
  • Ensure traceability of revisions, approvals, and controlled documentation
  • Support design transfer and sustaining engineering changes from a quality systems perspective
Performance Accountability - This role is accountable for:
  • QMS compliance status
  • CAPA cycle time and effectiveness
  • supplier quality performance
  • audit readiness and audit outcomes
  • documentation accuracy and traceability
  • quality system process compliance
Cross-Functional Interfaces - The Quality Manager will work closely with:
  • VP Operations
  • Director of Technical Operations
  • Regulatory Affairs
  • Engineering
  • Supply Chain / Procurement
  • Service Operations

Qualifications:
Required:
Education
  • Bachelor’s degree in Engineering, Life Sciences, Quality, Operations, or a related technical field
  • Equivalent relevant experience may be considered in lieu of degree
  • Advanced degree is a plus, but not typically required
Experience
  • 7+ years of progressive quality experience in a regulated manufacturing environment
  • 3+ years in medical device, diagnostics, or other highly regulated industry strongly preferred
  • Prior experience owning or administering a Quality Management System (QMS)
  • Demonstrated experience with CAPA, audits, supplier quality, and document control
  • Experience supporting FDA inspections and ISO 13485 certification audits
  • Prior startup or early-stage company experience strongly preferred
Technical / Functional Qualifications
Strong working knowledge of:o ISO 13485o 21 CFR Part 820 / FDA QMSR
   o CAPA systems
   o document control
   o training records
   o change control
   o supplier quality systems
   o audit management
Experience leading:
   o internal audits
   o external audits
   o supplier audits
   o corrective action programs
Experience with:
   o supplier qualification and SCARs
   o nonconformance and deviation management
   o root cause analysis
   o effectiveness checks
Preferred:
  • Experience with electromechanical medical devices or capital equipment
  • Familiarity with risk management / ISO 14971
  • Working knowledge of design controls
  • Experience partnering with Regulatory Affairs on submissions and inspections
  • Experience implementing or improving electronic QMS systems (eQMS)
Physical Requirements:
● Sitting, standing and walking, which may be for extended periods of time
● Lifting and carrying, up to 100 lbs
● Pushing, pulling, and reaching overhead
● Manipulation of objects and materials, including holding, grasping, turning, and touching
● Driving
● Stooping, crouching, kneeling
● Climbing ladders or stairs
● Hearing, in-person and through the telephone or electronic device (such as a computer)
● Speaking, in-person and through the telephone or electronic device (such as a tablet or computer)
● Visual acuity, both near (i.e. clarity of vision of approximately 20 inches or less) and far (i.e. clarity of
vision of approximately 20 feet or more)
● Regular and predictable attendance
The responsibilities outlined in this job description are intended to describe the general nature and level of work
performed by individuals assigned to this role. They are not intended to be an exhaustive list of all responsibilities,
duties, and skills required. Management reserves the right to amend and change responsibilities to meet
organizational needs as necessary.
SoftWave TRT is an equal opportunity employer. We make employment decisions solely based on business needs,
job requirements, and individual qualifications without regard to race, gender, religion, ethnicity, age, or any other

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