Careers

QC Incoming Inspector II

Summary of Primary Responsibilities:

The QC Incoming Inspector II completes all activities required to approve raw materials for use in product manufacture. The position also performs inspection activities during in-process manufacturing performs inspection and testing of components. The position revises and updates standard operating procedures as needed.

Specific Responsibilities:

  • Perform quality line clears and in process inspections during the inspection and packing processes according to specific SOP requirements
  • 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
  • Revise and review MPS documentation 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
  • Perform biennial review for designated procedures and MPS as needed
  • Documents; author and complete DCR as required
  • Document all work activities according to Good Documentation Practices
  • Maintain current training on all assigned procedures to include read & understood, skills development and classroom training activities as required
  • Participate in other projects as assigned

Job Complexity:

Works on assignments that are semi-routine/intermediate in nature but recognizes the need for occasional deviation from accepted practice.  The QC Incoming Inspector II normally follows established procedures on routine work, requires instructions only on new assignments.

Supervisory Responsibilities:

None

Required Qualifications:

  • Associates degree in the life science or relevant experience
  • 2 – 4+ years of experience in a cGMP facility or previous experience in a QA/QC role within the industry
  • Experience using Microsoft Office
  • Experience with ERP system for completion of inventory movement transactions

Desired Experience, Knowledge, and Skills:

  • Bachelor’s degree preferred
  • Experience working in a clean room environment
  • Ability to work autonomously, effectively manage time and deliver results on time
  • Excellent communication and documentation skills

 

Submit Your Resume