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QA Assistant in Dallas, TX at MEDISCA

Date Posted: 12/19/2018

Job Snapshot

Job Description

QA Assistant

The main purpose of this position is to review data results and maintain quality documents and procedures for the company that ensure compliance with established cGMP/GLP, ICH, USP/NF, and FDA regulatory requirements.

If you are an enthusiastic self-starter, goal driven, love quality and have an interest in the pharmaceutical industry, then we are looking for you!

The opportunity:

Analytical Data Review

  • Review data results to ensure for compendial procedure compliance.
  • Assist is the generation and review of Certificates of Analyses.
  • Review daily/weekly/monthly instrument verification checks and associated logbooks.

Ensure Compliance to the Quality System

  • Act as Sample Registrar for sample receipt and login procedures.
  • Maintain sample spreadsheets and input updates as needed.
  • Organize document archives by scanning completed data report, filing quality documents, purchase orders, service contracts, etc.
  • Maintain sample retain inventory and facility documents.
  • Assist Health and Safety Team with monthly duties.
  • Participate in quality activities and trainings.

Assist with other duties to support both quality and laboratory groups where needed.

Job Requirements

  • Sound knowledge of cGMP/GLP, ICH, USP/NF, FDA regulations
  • Excellent communication skills
  • Strong work ethic and reliable
  • Ability to build internal and external relationships
  • Excellent time management and organizational skills
  • Knowledge of Microsoft Office (Word, Outlook, Excel) required

  • 2 years experience in quality systems, quality assurance or quality control.
  • AA/B.Sc. in a Science related field.

If you feel that you have the skills required for this QA Assistant position, apply now by sending your resume to:

We thank all applicants for their interest; however, only candidates to be interviewed will be contacted.


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