QC Sampling & Inspection Technician

Unither Pharmaceuticals

Rochester, United StatesFull time
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Location
Rochester, United States
Job type
Full time
Posted
Oct 13
7 days ago
Career path

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About the company

Unither Pharmaceuticals

Pharmaceuticals · 1,001 to 5,000 employees

Unither Pharmaceuticals on LinkedIn

What you'll do

  • Samples and inspects incoming drug substances, raw materials, packaging components, and utilities; analyzes inspection results against specifications.
  • Maintains records, equipment schedules, and supplies, and supports investigations and development projects.

What you need

  • Must be able to gown to aseptic gowning standards.

Key skills

SOPscGMPsGDPsAseptic gowningData entryTroubleshootingEquipment calibration

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Read the full posting here
JOB SUMMARY: The QC Sampling & Inspection Technician performs sampling and inspection of incoming drug substances, raw materials, and packaging components while following applicable SOP’s and cGMPs. Sampling will also include sampling utilities such as purified water, water for injection, and pure steam. This role will also provide sampling & incoming inspection support for development projects. ESSENTIAL FUNCTIONS / RESPONSIBILITIES: Raw Material and Packaging Components Compliance Verified Performs routine sampling of raw materials and packaging components following applicable SOP’s and cGMPs. Performs utility sampling for purified water, water for injection, and pure steam. Analyzes the results of inspection tests to ensure conformity to specifications. Maintains and stocks supplies required to complete sampling and inspection activities. Identifies and communicates actual and potential problems. May support/provide input for investigations and troubleshooting, with supervision. Writes basic investigations with some assistance. Able to gown to aseptic gowning standards Documentation and Inspection/Sampling Environment Maintained to cGMP Standards Performs data entry and fills out paperwork following applicable SOP’s and cGMP/GDPs ensuring accuracy. Reviews colleagues work for accuracy in accordance with SOP’s and cGMP/GDP requirements. Maintains and updates training records in timeframe required by applicable procedures. Monitors and maintain equipment certification/calibration schedules Writes and participates in investigations as required

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