The QC Team Lead will be responsible for supervising the daily activities of the Quality Control department, ensuring that all inspections and quality checks are performed in accordance with company procedures and regulatory requirements. This role is crucial to maintaining product quality and compliance in a Class III medical device manufacturing environment.
Key Responsibilities
- Supervise and coordinate the daily activities of QC staff.
- Train QC personnel in inspection methods, QC procedures, handling of non-conforming materials, and product identification.
- Perform incoming inspections of raw materials, off-the-shelf parts, and custom-manufactured items to ensure they meet specifications.
- Conduct in-process inspections of products during manufacturing.
- Perform final inspection and release of finished products, including review of Device History Records (DHRs).
- Conduct environmental monitoring activities in the cleanroom, ensuring compliance with regulatory standards.
- Oversee maintenance and calibration of QC department equipment.
- Actively participate in Material Review Board (MRB) meetings and contribute to disposition decisions.
Requirements: - High School Diploma or equivalent required.
- Experience working in a cleanroom environment.
Proficient in the use of measuring tools (e.g., calipers, micrometers, gauges).
- Ability to understand and write documents in both English and Hebrew.
- Strong basic math and computer skills.
- Ability to read and interpret technical documents, drawings, and manuals.
- Hands-on experience in quality control within a regulated manufacturing environment (medical device industry preferred).
This position is open to all candidates.
