Job Details



Quality Control Data Reviewer


Quality Control Data Reviewer

 Primary Responsibilities and Essential Functions of the Position: Follow cGMP, cGLP, and OSHA gui...


Primary Responsibilities and Essential Functions of the Position:
  • Follow cGMP, cGLP, and OSHA guidelines with regard to work practices and safety.
  • Review data, reports and Standard Operating Procedures (initial creation and revisions), as required.
  • Write, and revise Standard Operating Procedures (SOPs), as required.
  • Review and revise laboratory systems.
  • Lead laboratory investigations.
  • May be required to Analyze raw, intermediate, final product and stability samples per compendial guidelines
  • May be required to Qualify, calibrate, and maintain chemical laboratory equipment as well as general laboratory maintenance.
  • Other duties as assigned.

 

Skills and Abilities Required:
  • Experience in USP analysis and review with HPLC and/or GC methods.
  • Experience preparing cGMP and other laboratory documents.
  • Proficient in chromatography software for analysis and review purposes.
  • Proficient in technical writing.
  • Proficient in leading and writing laboratory investigations.
  • Experience with cGMP and FDA regulations.
  • Excellent organizational skills.
  • Effective communication both verbally and written.
  • Proficient in Microsoft Word, Excel, and PowerPoint.

 

Minimum Education and Experience Required:
  • A Bachelor’s degree in Chemistry with a minimum of five (5) years of laboratory experience, preferably in the pharmaceutical industry; Master’s degree in Chemistry with a minimum of three (3) years laboratory experience, preferably in the  pharmaceutical industry; Ph.D. with a minimum of two (2) years laboratory experience preferably in a pharmaceutical industry.

 

Preferred Education and Experience:
  • 5-10 years of experience in a Pharmaceutical GMP facility.
  • 5-10 years of experience troubleshooting HPLC and GC.
  • Proficient in Chromeleon and Chemstation software.
  • 5-10 years of experience with ICH, DEA, Head Space, and IC regulation knowledge.
  • General knowledge of microbiology, for review purposes.
  • USP, EP, BP and JP methods of analysis, all or some.
  • Experience in Nasal Spray analysis and review.

 

Physical Requirements:
  • Ability to lift up to 35 pounds daily.
  • Standing for long periods of time on a regular basis; up to 8 hours per day.
Must be able to read, write, and communicate clearly

Location: Fenton - MO 

ZIP code:  63026

Reference: 108202

Secondary Reference:

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