Manager of Quality Assurance & Regulatory Affairs | AirStrip

NantHealth • San Antonio, TX

8d

About The Position

AirStrip is seeking an experienced Manager of Quality Assurance and Regulatory Affairs with organizational, communication, and problem-solving skills, including a sharp attention to detail and a results-oriented mindset. This role will lead continuous improvement initiatives across the Quality Management System for AirStrip, ensure compliance with global regulatory standards (including MDSAP, MDR, UKCA, ISO 13485, and QMSR), and apply a strong understanding of risk assessment to support business objectives. The ideal candidate is a creative, innovative team member who excels in collaborating with team members and mentoring others while driving high standards of quality, compliance, and operational excellence.

Requirements

• Bachelor's degree in Healthcare, IT, Quality, or related field (commensurate experience will be considered in lieu of degree)
• Minimum 5 years of experience managing QA / RA in a medical device company
• Minimum 5 years of experience understanding guidance’s from FDA and international regulatory agencies.
• Strong organizational, planning, and follow-up skills
• Strong interpersonal communication (written and verbal)
• Effective problem-solving skills; results-oriented
• Outstanding attention to details
• Creative and innovative thinker
• Coaching and mentoring for direct reports
• Continuous improvement for QMS
• Proven compliance with the current and applicable standards and regulations such as MDSAP, MDR, UKCA, ISO 13485, QMSR, etc.
• Strong understanding of risk assessment

Responsibilities

• Develop, implement, and maintain QSDs in order to assure compliance of the Company’s Quality System with MDSAP, 21 CFR Part 820 and any other FDA guidance and regulations related to SaMDs
• Participate during audits conducted by Notified and Regulatory bodies by providing professional support and expertise for Quality Assurance and Regulatory Affairs topics
• Act as team member of New Product Development (NPD) or Existing Product Enhancement (EPE) Teams during all phases of the development of the Design History Files (DHFs)Technical Files (TFs) as wells as Risk Management, Clinical Evaluation or Post-Market Surveillance Files.
• Participate in the Nonconforming Product and Complaint Processes in order to identify, document, evaluate, segregate and disposition in a timely manner the Nonconforming Product and/or Customer Complaints.
• Solve the systemic Product Non-Conformances (NCs) through the Corrective Actions Preventative Actions (CAPA) Process in order to eliminate or prevent the occurrence of these NCs
• Participate in and ensure timeliness of Internal and Supplier Audits according to the Company’s Audit Programs and current standards and regulation requirements
• Organize and coordinate the CAPA, Complaints, Clinical Evaluation and Post-Market Surveillance data collection, monitoring, analysis and report for the Management Review meetings
• Maintain international authorizations including but not limited to ISO 13485:2016, MDSAP, MDD/ MDR Certifications, UKCA, and CMDCAS registrations, as well as the regulations that apply to any area the Company determines are in its best interest.
• Establishing compliance “knowledge base” that can be mined to extract compliance statistics and current regulations

What This Job Offers

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