Provides analytical chemistry support and/or remediation for chemistry-related projects related to Client products currently on the market, as well as new product development. Participates in stability testing programs supporting approval of process/product design changes and supports development/validation of analytical methodologies for incoming raw materials, in-process, and finished product release testing.
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Perform chemistry and performance testing
Conduct data review and entry
Generate protocols and reports
Provide laboratory maintenance and support
Support stability testing programs for process/product design change approvals
Develop and validate analytical methodologies for raw materials, in-process, and finished product release testing
Discuss scientific strategies/results and interact with other functional areas (Regulatory, Manufacturing, Quality)
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2-4 years of experience in pharmaceutical analytical chemistry (essential)
Hands-on experience with wet-chemistry and instrumental techniques (pH, titration, UV-Vis, GC, HPLC)
Experience working within an FDA-regulated environment and GMP documentation requirements
Previous experience writing scientific protocols and reports
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Standard scientific method and techniques within respective discipline
Excellent scientific writing skills
Multi-tasking across various activities
Troubleshooting and problem-solving
Interpreting instructions in written, oral, diagram, or schedule form
Numbers & Facts
Location
Vernon Hills, IL
Skills
Analytical Chemistryunmatched
Analytical Method Developmentunmatched
Analytical Method Validationunmatched
Chemistryunmatched
Data Entryunmatched
High Performance Liquid Chromatography (HPLC)unmatched