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QC Incoming Inspector , 1st Shift

Job in Bedford, Middlesex County, Massachusetts, 01730, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-03-01
Job specializations:
  • Quality Assurance - QA/QC
    Quality Technician/ Inspector, Quality Control / Manager, QA Specialist / Manager
  • Manufacturing / Production
    QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 40000 - 55000 USD Yearly USD 40000.00 55000.00 YEAR
Job Description & How to Apply Below
Position: QC Incoming Inspector I, 1st Shift

Role Summary

The QC Incoming Inspector completes all activities required to approve raw materials for use in product manufacture. The position also performs inspection activities during in-process manufacturing.

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
  • 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
  • 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
Qualifications
  • Required:

    Associates degree in the life science or relevant work experience
  • 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
Skills
  • Bachelor’s degree preferred
  • Experience working in a clean room environment
  • Excellent communication and documentation skills
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