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Quality Assurance Specialist

Job in Suwanee, Gwinnett County, Georgia, 30174, USA
Listing for: Femasys Inc.
Full Time position
Listed on 2026-09-17
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 65000 - 90000 USD Yearly USD 65000.00 90000.00 YEAR
Job Description & How to Apply Below

Femasys is a dedicated team of experts united by a shared passion to advance technologies that address genuine gaps in women’s health.

Open Positions Current openings.

Position: Quality Assurance Specialist Location: Suwanee, GA
Job :157 # of Openings:1 About Femasys Femasys is a pioneering biomedical company focused on advancing women's health by developing and commercializing innovative, accessible solutions for reproductive care. Our product portfolio includes breakthrough technologies for permanent contraception, fertility enhancement, and diagnostic procedures - providing meaningful options for both patients and healthcare providers.

Position Summary We are looking for a Quality Assurance Specialist who thrives in a small, fast-paced environment and wants to play a hands‑on role in bringing innovative medical devices from concept to market. This position is responsible for supporting and maintaining the Quality Management System (QMS) to ensure compliance with applicable regulatory requirements, industry standards, and company procedures. This role serves as the primary owner of the Customer Complaint Handling System and the Equipment Maintenance and Calibration Program, ensuring processes are effectively implemented, monitored, and continuously improved.

The QA Specialist collaborates cross-functionally with Manufacturing, Engineering, Regulatory Affairs, Customer Service, and Operations to maintain product quality, regulatory compliance, and patient safety.

  • Quality Management System Support
    • Support the implementation, maintenance, and continuous improvement of the Quality Management System (QMS).
    • Ensure compliance with FDA Quality System Regulations (21 CFR Part 820), ISO 13485, and other applicable regulatory requirements.
    • Prepare, review, and maintain quality procedures, work instructions, forms, and records.
    • Assist with internal and external audits, including preparation, execution, response, and follow‑up activities.
    • Support CAPA, nonconformance, risk management, and change control activities as assigned.
    • Monitor quality metrics and generate reports to support management review activities.
  • Customer Complaints
    • Serve as system owner for the Customer Complaint Handling process.
    • Receive, document, investigate, and process customer complaints in accordance with company procedures and regulatory requirements.
    • Perform ERP transactions for complaint returns.
    • Perform preliminary complaint assessments and coordinate investigations with cross‑functional teams.
    • Ensure complaint records are complete, accurate, and maintained in accordance with retention requirements.
    • Monitor complaint timelines to ensure timely closure and regulatory compliance.
    • Analyze complaint data and trends to identify recurring issues, opportunities for improvement, and potential CAPA inputs.
    • Prepare complaint metrics and summaries for Management Review meetings.
    • Support regulatory inspections and audits involving complaint handling activities.
  • Equipment Maintenance and Calibration System
    • Serve as system owner for the Equipment Maintenance and Calibration Program.
    • Maintain the inventory list of production, inspection, test, and monitoring equipment.
    • Coordinate preventive maintenance and calibration activities with internal personnel and external service providers.
    • Verify equipment calibration status and ensure traceability to recognized standards when applicable.
    • Review calibration certificates and maintenance records for completeness and compliance.
    • Investigate overdue calibrations, maintenance deviations, or equipment‑related quality issues.
    • Ensure equipment is appropriately identified, labeled, and controlled to prevent unintended use of out‑of‑calibration equipment.
    • Monitor program performance metrics and identify opportunities for…
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