Quality Manager

SoftWave TRT • Marietta, GA

2d

About The Position

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.

Requirements

• Bachelor’s degree in Engineering, Life Sciences, Quality, Operations, or a related technical field
• Equivalent relevant experience may be considered in lieu of degree
• 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
• Strong working knowledge of:o ISO 13485o 21 CFR Part 820 / FDA QMSR
• CAPA systems
• document control
• training records
• change control
• supplier quality systems
• audit management
• Experience leading:
• internal audits
• external audits
• supplier audits
• corrective action programs
• Experience with:
• supplier qualification and SCARs
• nonconformance and deviation management
• root cause analysis
• effectiveness checks

Nice To Haves

• Advanced degree is a plus, but not typically required
• 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)

Responsibilities

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Manager