Inspector; QA Manufacturing - 1st Shift (7:30AM - 4:00PM)

CONTRACT PHARMACAL CORP•Town of Smithtown, NY

About The Position

The Inspector, QA Manufacturing is responsible for maintaining product quality throughout all phases of manufacturing in accordance with current good manufacturing practices. The role performs in-process inspections and monitoring, reviews manufacturing documentation, supports sampling and environmental monitoring, and provides quality assurance support to production operations. The position works in production facilities and may require movement between production areas or sites. Work hours, shifts, and location may change based on business needs and management discretion. The role has no supervisory responsibilities.

Requirements

  • High school diploma or GED.
  • Ability to read, write, and communicate effectively.
  • Self-motivated, with the ability to work in a fast-paced environment and handle multiple tasks simultaneously.
  • Excellent organizational skills and attention to detail.
  • Able to reach with arms and use hands and fingers to handle or feel objects and tools.
  • Able to stoop, kneel, crouch, stand, bend, sit, talk, hear, and climb stairs and ladders.
  • Able to lift and/or move up to 50 pounds.
  • Able to work in production facilities near heavy machinery, loud noises, and pharmaceutical powder dust.
  • Gowning as required by GMPs and/or SOPs, and PPE as needed.

Nice To Haves

  • Knowledge of good manufacturing practices and good documentation practices.

Responsibilities

  • Perform in-process monitoring of manufacturing operations, including weight, thickness, hardness, disintegration, and friability.
  • Perform duties using good documentation practices.
  • Collect in-process and finished product samples as required.
  • Support microbiological sample collection according to procedures.
  • Perform room inspections and clearances as required.
  • Perform batch record release for Commercial and IP batch records.
  • Perform AQL sampling and inspections as required.
  • Identify and report non-conformances or discrepancies to management, if applicable.
  • Review that production is following general SOPs.
  • Assist with initial and ongoing employee training.
  • Support environmental monitoring activities, including water and air sampling.
  • Provide additional QA technical support to the Coating Department.
  • Review batch record documentation.
  • Issue QMS forms to production as required.
  • Verify scale weights daily.
  • Maintain QA supplies.
  • Review weekly pest control logs.
  • Transmit samples to QC and Account Services.
  • Review the Maintenance grounds logbook.
  • Audit facility fire extinguishers monthly.
  • Perform other responsibilities as assigned by Senior Management.
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service