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Define and execute the companys quality vision, strategy, and objectives specifically for hardware products in the security systems and IoT sectors.
Oversee QA / QC for hardware products including sensors, cameras, and access control devices.
Lead quality efforts with subcontractors, ensuring compliance with standards (e.g., UL, CE, ISO 9001).
Manage supplier qualification, audits, and lead continuous improvement initiatives.
Collaborate with R D, engineering, and manufacturing teams to ensure design for manufacturability.
Monitor KPIs, drive root cause analysis, and lead CAPA (Corrective and preventive action) / 8D investigations processes.
Mange HW / production related customer complaint/ SCAR, RMA and MRB (Material review board) process.
Review, approve and support products change request activities.
Oversee production quality control activities, including receivin

o Manage SW QA and version approval process
o Manage HW QA approval for Amimon's products
o Handle and manage medical V&V including regulation documents, V&V protocol design and execution.

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.