• Inspects and tests incoming chemicals and in-process product components using analytical analysis and instrumentation (HPLC, UPLC, MS, LC/MS, UV-Vis, etc.).
• Supports and executes protocols for analytical test methods and the ability to aid in the transfer of methods to Quality Control.
• Identifies non-conforming material and documents conditions in Trackwise deviation system. Maintains / updates the material status of quarantined and non-conforming materials in the ERP/FTPS database.
• Support product and process improvement, and engages in special projects as needed in QC and other areas.
• Provides technical writing as needed; maintains trending and interpretation of KPI and other data as needed.
• Updates procedures and/or specifications in the Document Control System; Performs Verification / Validations of scientific methods, systems, or equipment.
• Manages and executes MT (micro-use) preparations and scheduling activities for MT tests.

• Requires a 4-year degree in chemistry, biology or related scientific field.
• Requires a minimum of 3 years related experience with proficiency in the use of analytical instrumentation (HPLC, UPLC, FTIR, UV-Vis, etc)
• Experience in a cGMP / FDA regulated environment is highly preferred.
• Requires strong computer skills including Microsoft Office Package (Excel, Word, etc.).
• Must possess strong mathematical and analytical skills.
• Must be able to demonstrate flexibility in responding to unexpected demands. Must also be able to work in team environment, building effective working relationships.

• Domestic travel required 10% of time
• International travel required <5% of time

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