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Quality Assurance Inspector

Job in Commack, Suffolk County, New York, 11725, USA
Listing for: Evolving Solution Services
Full Time position
Listed on 2026-09-10
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Production QC/QA
  • Manufacturing / Production
    Production QC/QA
Salary/Wage Range or Industry Benchmark: 22 - 25 USD Hourly USD 22.00 25.00 HOUR
Job Description & How to Apply Below

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Quality Assurance Inspector

Full Time Commack, NY, US

3 days ago Requisition

Salary Range: $22.00 To $25.00 Hourly

Principal Duties and Responsibilities of The Position General
  • Monitor all GMP activities in assigned areas and throughout Gemini facilities.
  • Monitor temperature and humidity in all production and warehouse areas throughout Gemini facilities.
  • Perform room clearance checks throughout manufacturing and packaging areas.
  • Have basic familiarity with equipment used in the manufacturing and packaging of pharmaceuticals.
  • Perform room clearance checks of manufacturing, and packaging rooms as applicable.
  • Perform daily inspection checks to pest control stations.
  • Ensure product quality, through visual inspection of goods in accordance with the ANSI/AQL sampling standard and requirements to determine a final disposition of finished bulk and/or packaging components.
  • Should be able to wear filtering facepiece (dusk mask, surgical mask, respirator) throughout the day.
  • Conduct Special Projects and or perform other functions as instructed by Quality Assurance Management.
Pharmacy
  • Ensure raw materials are received, sampled, and status control per procedure.
  • Monitor Sampling and Pharmacy operations.
  • Creation of raw material inventory cards upon QC release of materials.
Manufacturing
  • Perform manufacturing checks of raw materials, product blends and capsule shells at set up as well as throughout manufacturing runs.
  • Perform manufacturing checks during compression process, and limited to weight, hardness, thickness, and physical appearance checks.
  • Perform manufacturing checks during encapsulation process, including but not limited to weight check, and physical appearance checks.
  • Pull test samples for Quality Control Laboratory
  • Perform process checks during bulk inspection process.
Packaging
  • Perform verification of packaging components at the line set up as well as throughout the packaging run.
  • Perform verification of packaging components at the line set up as well as throughout the packaging run.
  • Perform labels and carton conformation checks at start up as well as during packaging runs.
  • Performs half-hour checks on products during the packaging process, including but not limited to:
    Label checks, cotton checks, barcode checks, product count, product name, proper seal etc.
  • Performs clean room checks every hour to ensure there are no pills on the floor, no extraneous packing debris, or spillage.
  • Pull Packaging retain samples.
Receiving
  • Sampling, Inspection, and Release of Component Materials; status monitoring of components
  • Review packaging component inventory forms for accuracy and completion; resolve inventory discrepancies; approve and close out forms.
  • Perform in-process inspection checks in the inspection department.
Required Skills and Experience
  • Strong verbal and written communication skills
  • Strong organizational skills and ability to prioritize and multi-task.
  • Excellent analytical, problem-solving, and decision-making skills
  • Physical Requirements – ability to bend, twist, reach, climb ladders, lift materials up to 50 lbs.
  • Must have good vision, aided by glasses, if necessary
  • Must successfully pass the Color-Blind Test as (normal color vision)
Additional Skills
  • Bilingual is a plus.
  • Experience in a pharmaceutical/ Food Safety (HACCP) environment preferred.
  • Quality training or equivalent continuous improvement experience preferred.
  • In-depth knowledge of cGMPs, FDA, CFR requirements OSHA, fire and general safety preferred.
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