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Associate QC Scientist

 

Your Role:  To perform Quality Control activities in support of raw materials in support of cGMP products, including routine testing (in-house and compendial) and peer review of data.  

 

Essential Job Functions: 

  • Perform routine testing of raw materials samples through adherence to applicable GMP requirements. Assure adequately trained to perform tasks/assignments.
  • Utilize written procedures to perform routine and non-routine product testing.
  • Work in accordance with current GMPs and demonstrate proper laboratory safety and housekeeping practices.
  • Participate in method development and validation activities to support product testing, if needed.
  • Contribute to support function of the laboratory through participation in laboratory audits to maintain compliance.

 

Who You Are:

 

Basic Qualifications:

BA/BS in the Life or Physical Sciences or equivalent relevant experience required.

 

Preferred Experience:

2 years previous laboratory experience with titrationsis 

2 years experience preferable in a GMP environment utilizing compendial assays.

 

Desired Knowledge and Skills:

  • General laboratory techniques (theory and practice)
  • Experience with instrumentation used in chemical analysis, such as FT-IR, Titrations, UV-Vis Spectrophotometer, TOC, Karl Fischer, and pH meter.
  • Working Knowledge of Good Manufacturing Practices for pharmaceutical manufacturing (21 CFR 210 & 211 and/or ICH Q7A)
  • Knowledge of Microsoft Word, Excel and Access
  • Strong time management, Troubleshooting Skills, verbal and written communication skills

 

 

Job Requisition ID:  187889
Location:  St. Louis
Career Level:  D - Professional (4-9 years)
Working time model:  full-time


Job Segment: Chemistry, Housekeeping, Scientist, Pharmaceutical, Laboratory, Science, Healthcare

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