Medix Staffing Solutions

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QC Inspector, Pharmaceutical

at Medix Staffing Solutions

Posted: 4/27/2019
Job Status: Full Time
Job Reference #: J3R3RR665GHG53W2YVH
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Job Description

QC Inspector, Pharmaceutical

Location: Lakewood, NJ

Pay: $18 - 21/hr (based on experience)

Hours: 1st / 2nd shift (Full-time plus OT)

Benefits: Dental/Health/Vision/401k

Quality Control Incoming Inspectors conduct raw material, packaging and component sampling component, label and packaging inspection and dimensional testing to ensure products comply with Company policies and standard operating procedures (SOPs) and Good Manufacturing Practices (GMP) requirements. They issue and control the labels and packaging inserts and are responsible for following all quality control procedures and ensuring all documentation meets cGMP standards. They are responsible for cleaning and environmental monitoring their respective work area as required.

  • Perform Incoming tasks including, sampling, inspections, and quality attributes testing designed
  • Monitor product quality through the performance of required visual testing and additional testing as needed. A brief description of the job's primary purpose or contribution to the department or organization
  • Perform routine inspections on the on all incoming components. .
  • Ensure routine compliance of day to day activities in the sampling and inspection areas; working with operations personnel to achieve compliance.
  • Review the required paperwork for accuracy and compliance, upon completion of the activity.
  • Report non-conformances associated with components, labels, packaging and raw materials etc.
  • Collect representative samples for testing and retention, and ensure all relevant paperwork is complete. Submit samples/resamples to laboratory in a timely fashion to meet production needs.
  • Inspect and approve packaging components.
  • Apply Rejection stickers to rejected materials based on Quality Assurance approved Notice of Rejection.
  • Stage label and inserts on production lines, issuing reports and verifying customer and Renaissance part numbers and comparing information to the staging sheet. Return unused labels and inserts or have them destroyed when requested by customer.
  • Process and distribute samples to other teams for evaluation and testing, as required.
  • Ensure all work performed is documented accurately and completely on forms, logs and other documents.
  • Maintain a clean and safe environment in compliance with State and Federal regulatory guidelines.
  • Perform other duties and responsibilities as assigned.
Reference number: 81673
- 2+ years experience in QC Inspection • Pharmaceutical / Medical device preferred