Description
Our client, a leader in the biomedical industry, has an immediate opening for a QC Inspector. This role will perform quality line clears and in process inspections during the inspection and packing processes according to specific SOP requirements.
Responsibilities:
- Issue lot numbers and control labels for incoming raw materials; perform inspections per internal procedures and specifications
- Release approved raw materials for use in manufacturing process to include completion of associated documents, notice of approval form (bin card), and relabeling of inventory
- Review MPS of other incoming inspectors for approval and release
- Monitor and perform annual retain inspection; coordinate required retesting with QC; complete required documentation
- Perform OOS investigations and participate in MRB as required for rejected materials
- Perform as SME for the function and provide training as required to new employees, contractors, and other QA personnel
- Document all work activities according to Good Documentation Practices
- Participate in other projects as assigned
Requirements:
- Associate's degree in the life sciences or relevant work experience; Bachelor's degree preferred
- 0–1 year of experience in a cGMP facility or previous experience in a QA/QC role within the industry; internship experience considered
- Experience using Microsoft Office or an ERP system
- Experience working in a clean room environment preferred
- Excellent communication and documentation skills preferred