QC Inspector

The Quality Control Inspector role is essential in ensuring incoming, in-process and finished medical devices meet specifications. The Quality Control Inspector provides total manufacturing quality inspection services including quality inspection, quality control, sampling inspection, documentation and record review and approval. Adhering to Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) is essential to maintain all documentation necessary to ensure conformity to specifications and traceability of records.

Essential Duties and Responsibilities:

Responsible to perform set-up, in-process dimensional and visual audits to ensure compliance to all specifications and DMR. Responsible to record all the test results and the activities in the relevant documents as part of the DHR
Responsible to verify that all acceptance test results meet the requirements according to the procedures and specifications.
Responsible to verify that all acceptance test results follow GMP and GDP guidelines. Conform with and abide by all regulations, policies, work procedures, instruction, and safety rules.
Responsible for the approval of line clearance at the production lines, testing stations and cleanroom.
Responsible for approving raw materials.
Responsible to verify stored raw material, approved devices and subassemblies and rejected materials are identified and traceable as required in applicable procedures and specifications.
Responsible for nonconformities handling inside the production room and for the MRB cage at Raanana warehouse.
Responsible for incoming inspection for R&D items and materials that are in use to support devices samples build sand meet customer demands during development stages.
Determine whether a Non-Conformance (NCR) has occurred and follow established procedures to initiate corrective actions.
Perform other duties as assigned based on business needs.