Join a mission-driven organization dedicated to improving human health
Job Summary
Join a mission-driven organization dedicated to improving human health.
As a Quality Engineering Supervisor, you will support the manufacturing of medical devices and clinical diagnostic reagents that empower customers to detect disease, accelerate research, and protect patient health.
Your leadership will directly contribute to delivering safe, compliant, and high-quality products that make a real-world impact.
Matching Summary
Join a mission-driven organization dedicated to improving human health.
Skills & Requirements
Must-have
Quality assurance processes compliance
Team leadership and supervision
CAPA and root cause analysis
Regulated manufacturing environment
Quality documentation review and approval
Data-driven quality improvement
Cross-functional collaboration
Nice-to-have
Lean and Six Sigma methodologies
Risk-based quality methodologies
Statistical techniques familiarity
Excellent communication skills
Strong problem-solving abilities
Organizational and prioritization skills
Commitment to patient safety
Key Requirements
Bachelor’s degree in Engineering or Life Sciences preferred
Experience in Quality Engineering for medical devices or IVD
FDA QSR, ISO 13485, ISO 14971, GMP knowledge
Experience in team supervision or technical leadership
Legal authorization to work in the US without sponsorship
Ability to pass background check and drug screening
Work Rights
Must be legally authorized to work in the United States without sponsorship