Kelly Services Quality Control (QC) Inspector in Clearwater, Florida

Quality Control (QC) Inspector

Pharma Exp

Contract to Perm

1st shift

Pay is $14 an hour during contract


  • Perform on-line inspection activities including appropriate documentation as required. These activities include pre- and post-line clearances, inspection of staged components for correctness, in-process sample evaluation, finished goods inspection, verification of line clearances at appropriate times.

  • Prepare QA documentation for upcoming lots.

  • Verify release and correct staging for materials prior to weighing for the compounding department.

  • Release compounding bulk to packaging.

  • Perform initial review of compounding and packaging batch records.

  • Perform review of purified water use log.

  • Ensure that corrections are made, and mentor the guidance of corrections found within packaging batch records, and compounding batch records.

  • Assist in verification of product, raw material, and component expiration dates.

  • Initiate the collections of finished goods sampling for special/additional testing.

  • Obtain, prepare, and store all retain samples. Maintain the retain areas in a neat and orderly manner. Obtain, prepare, and ensure accuracy of stability samples as directed by the Quality Control Department.

  • Obtain, prepare, and submit specified laboratory samples during packaging for chemical and microbiological testing as required.

  • Perform Raw Material Sampling and submit samples to Laboratory for testing.

  • Inspection of Labeling materials, and recommend disposition of said labels.

  • Monitor the compounding of controlled drugs and other compounding activities as required by procedure(s).

  • Perform annual retain sample review and assist with retain destruction.

  • Assist in taking inventory of materials, as required.

  • Follow all SOP’s (Standard Operating Procedures) pertinent to quality assurance inspection.

  • Attend training sessions in order to maintain and increase skills and knowledge of current good manufacturing practices (cGMPs) and safety awareness.

  • Perform other duties as assigned by the Quality Assurance Supervisor.


  • An Associate Degree is required. Detail oriented, and proficient in mathematics. Two years’ experience in pharmaceutical industry preferably in quality assurance functions and a working knowledge of cGMP’s.


  • Prolonged periods of sitting or standing or constant walking. The ability to lift up to 25 pounds. The ability to climb ladders or stairs while carrying up to 25 pounds.


  • Reports directly to the Quality Assurance Supervisor.

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With Kelly, you’ll have access to some of the world’s highest-regarded scientific organizations—providing you with opportunities to work on today’s most challenging, research-intensive, and relevant projects. Our connections can lead you to innovative scientific pursuits you’ll be proud to help advance. We work with 95 of the Fortune 100™ companies, and found opportunities for more than 11,000 scientific professionals last year.

You pursued a career in science to fuel your quest for knowledge and your desire to make the world a better place. Let Kelly fuel your career—connect with us today.

AboutKelly Services ®

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