QC Team Lead

Aurora Lifesciences; Yorkshire, Northern (VA, KY); Hybrid; USD 90,000 - 120,000; Full time

Job summary

Aurora Lifesciences in Virginia seeks a hands-on Team Leader, Quality Control to guide daily inspection and release activities, coordinating workload and providing technical direction for incoming, in-process, and final inspection. The role requires strong knowledge of ISO 13485, regulatory requirements, and a proven ability to lead a cross-functional team in a regulated medical device environment.

You will drive quality, safety, and continuous improvement while ensuring compliant documentation

Qualifications

• HNC/HND or degree in Engineering, Quality, Manufacturing, or a related technical discipline.
• Experience in quality control, receiving inspection, product inspection, or incoming quality in regulated manufacturing.
• Experience in medical device manufacturing is desirable.
• Previous experience in a team leader or shift leadership role.
• Working knowledge of ISO 13485, EU MDR, and FDA 21 CFR Part 820.
• Formal quality system or regulatory training would be advantageous.

Responsibilities

• Lead and support a team of Quality Control and Receiving Inspection personnel.
• Allocate daily workload, provide technical guidance, and support shift priorities.
• Act as a technical escalation point for inspection queries, specification interpretation, and non-conformance decisions.
• Ensure incoming materials, components, sub-assemblies, and finished products are inspected, tested, documented, and dispositioned in line with approved procedures.
• Review and authorise inspection records within delegated authority.
• Support final product inspection, testing, verification, and release activities.
• Review supplier documentation and support receiving inspection requirements.
• Conduct first article inspections against specifications, drawings, and engineering requirements.
• Identify training needs and support team qualification activities.
• Monitor inspection performance, resource needs, and non-conformance trends.
• Contribute to continuous improvement across inspection, manufacturing, and quality processes.
• Promote a culture of compliance, accountability, safety, and continuous improvement.
• Work closely with Manufacturing, Engineering, Quality Assurance, Supply Chain, and other business functions.

Skills

People leadership

Team coordination

Technical judgement

Attention to detail

Cross-functional collaboration

Communication skills

Education

Engineering/Quality degree

Job description

Role Summary

An established medical technology manufacturer is seeking a Team Leader, Quality Control to support its inspection and quality control operations. This hands-on role will provide daily leadership, technical guidance, and workload coordination for a team responsible for incoming inspection, product inspection, and final release activities.

The role is suited to an experienced quality professional with strong knowledge of regulated manufacturing environments and applicable quality system requirements, including ISO 13485, EU MDR, and FDA 21 CFR Part 820.

Key Responsibilities

• Lead and support a team of Quality Control and Receiving Inspection personnel.
• Allocate daily workload, provide technical guidance, and support shift priorities.
• Act as a technical escalation point for inspection queries, specification interpretation, and non-conformance decisions.
• Ensure incoming materials, components, sub-assemblies, and finished products are inspected, tested, documented, and dispositioned in line with approved procedures.
• Review and authorise inspection records within delegated authority.
• Support final product inspection, testing, verification, and release activities.
• Review supplier documentation and support receiving inspection requirements.
• Conduct first article inspections against specifications, drawings, and engineering requirements.
• Identify training needs and support team qualification activities.
• Monitor inspection performance, resource needs, and non-conformance trends.
• Contribute to continuous improvement across inspection, manufacturing, and quality processes.
• Promote a culture of compliance, accountability, safety, and continuous improvement.
• Work closely with Manufacturing, Engineering, Quality Assurance, Supply Chain, and other business functions.

Required Experience

• HNC, HND, degree, or equivalent qualification in Engineering, Quality, Manufacturing, or a related technical discipline.
• Experience in quality control, receiving inspection, product inspection, or incoming quality within a regulated manufacturing environment.
• Experience in medical device manufacturing is desirable.
• Previous experience in a team leader, supervisory, or shift leadership role.
• Working knowledge of ISO 13485, EU MDR, and FDA 21 CFR Part 820.
• Formal quality system or regulatory training would be advantageous.

Key Skills

• Strong people leadership and team coordination skills.
• Good technical judgement and attention to detail.
• Ability to interpret specifications, inspection criteria, and technical drawings.
• Clear written and verbal communication skills.
• Ability to prioritise work and deploy resources effectively.
• Confident working with cross-functional teams.
• Hands-on, proactive, and comfortable working in a regulated manufacturing environment.
• Strong commitment to quality, compliance, safety, and continuous improvement.

Ideal Candidate Profile

The ideal candidate will be a practical and detail-focused quality professional with proven experience in regulated manufacturing and inspection environments. They will combine strong technical inspection knowledge with the ability to lead people, manage priorities, and support a culture of compliance and continuous improvement.

They will be confident working in a cleanroom and office-based environment, comfortable interpreting specifications and technical drawings, and able to act as a trusted escalation point for inspection-related decisions. Above all, they will demonstrate a strong commitment to quality, safety, teamwork, and delivering products that meet the highest regulatory and customer expectations.