QC Inspector Job at Regal Staffing Services, Midlothian, TX

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  • Regal Staffing Services
  • Midlothian, TX

Job Description

Job Description

Job Description

Regal Staffing Services now hiring a Quality Control Inspector located in the Midlothian, TX area.

If you would like to apply or have any questions, please call (469) 310-5850 and ask for either Juana or Esperanza

Shifts/Pay Rate : Monday - Friday (4:30am to 3:30pm): $19.00hr

Responsibilities :

  • Oversees logs and procedures and ensures Q.C. and Production are abiding by GMP and GLP company rules set forth by company SOPs. Ensuring things are made right in the first place is the best way of preventing out of -specification products
  • Reviews and approves the Production filling batch records.
  • Checks and audits the documents for accuracy and GMP compliance during and at the completion of filling.
  • Checks and confirms that the correct components and compounding batch have been set-up and are being used on the appropriate packaging line.
  • Reviews the data reported by the mechanics, machine operators, and line leads to ensure that the information is correct and entered appropriately.
  • Responsible for placing compounded batches and finished goods that do not conform to company specifications into Quarantine status with applicable labeling.
  • Reports any quality issues to Quality management and participates in investigations, as necessary.
  • Performs daily housekeeping audits of the Production area logbooks and reports results to Quality management.
  • Supports GMP training of employees.
  • Participates in Quality System audits as directed by Quality management.
  • Complies with Health, Safety, and Environmental responsibilities for the position.
  • Inspects the production lines to ensure that both Production and Quality control personnel are following the required SOP to perform their jobs.

Requirements :

  • Minimum 6-months -1 year of hands-on experience as Quality audit/inspector in cGMP environment; preferably in pharmaceutical, biomedical, or medical device field (regulated industry).
  • Experience with batch record keeping, CAPA initiation, and deviation investigation.
  • Fluent in reading, writing, and speaking the English language, as well as having experience with technical writing (knowing Spanish is a plus)
  • Proficient in MS Office (Word, Excel, Access and PowerPoint) and e-mail.
  • The employee must occasionally lift and/or move up to 10 pounds.
  • Stable work history
  • Pass background check and drug screen

How to Apply :

  • Fill out our official application online at (be sure to select " Dallas " as your branch).
  • If you have any questions, please contact us at (469) 310-5850 .

Job Tags

Immediate start, Shift work, Monday to Friday,

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