Engineer III, Supplier Quality

Qualifications

• Bachelor’s Degree in Science, Health, or Engineering
• A minimum of four years of experience in a supplier‑interacting role within a professional environment with an established QMS
• A minimum of four years of experience in an FDA (or other Competent Authority) regulated environment
• Experience navigating Quality, Regulatory, and Industry standards in the medical device or pharmaceutical spaces

• Auditor Certification (e.g. CQA, CMDA) or auditor experience
• Experience with standards such as ISO
  9001, ISO
  13485, ISO
  17025, or others
• Experience with DQ / IQ / OQ / PQ and overall Process Validation (PV) navigation
• Experience with controlled environments, such as controlled room temperature, continuous monitoring, and clean rooms or clean spaces
• Corrective Action / Preventative Action (CAPA) navigation
• Nonconformance or Deviation investigations, including Root Cause Analysis (RCA)
• Experience in Quality Audit response preparation and implementation of Action Items
• Experience in Change Control / Change Management navigation
• Experience with regulations such as 21
  
  CFR
  210, 21
  
  CFR
  211, or 21
  
  CFR
  820
• Technical Writing ability, consistent with Enable and industry expectations
• Adaptable Communication ability to interact with persons intra‑ and inter‑departmentally, suppliers, and other Enable partners
• Self‑manage, prioritize, and ensure efficient time‑management of assigned tasks
• Employ positive influence to lead suppliers in a parallel path with Enable objectives
• Demonstrate Business Acumen, including strategic planning and challenge resolution
• Operate with the highest integrity in representation of the Supplier Management department and Enable

• Work in Quality and Manufacturing departments when required
• Ability to remain sedentary for extended periods of time
• Light work that includes moving objects up to 40 pounds
• Position requires being physically present on the premises during regular company hours or as approved by management
• Ability to travel approximately 20% as needed

• Maintain the Approved Supplier List (ASL) and support ASL activities (e.g. form review and routing)
• Independently and/or collaboratively with the Manager, Supplier Quality, as needed or directed, provide guidance to the Enable team on the pathway for Supplier Qualification, consistent with site procedures
• Navigate SCARs and/or Quality Alerts with the Enable team and suppliers to ensure robust documentation and closure
• Support the scheduling, performance, and/or documentation of on‑site and/or remote Quality audits
• Support the supplier evaluation and performance documentation (e.g. Supplier Scorecards)
• Apply a risk‑based perspective with an understanding of Critical, Major, Minor, or non‑GxP classification, when assessing new or approved suppliers to Enable
• Create and revise procedures to support the Supplier Management department and Enable
• Drive or assist, as needed, with the responses and action implementation associated with CAPAs, Nonconformances, Quality Audits, Change Control / Change Management, and other QMS elements
• Ensure accuracy of all documentation, including traceability or linkage of supplier documentation in both physical and electronic platforms (e.g. paper and SAP)
• Provide routine updates to department leadership, including escalation of any supplier‑related challenges (e.g. component quality concerns)
• Develop and nurture strong collaborative relationships with the Enable supplier network to support continuous improvement efforts