Job Description
Description
Run analytical testing for release and stability testing
Support method optimization
Help with method qualification and method validation for analytical methods for internal and external contract laboratories
Review and write protocols, test methods, and SOPs
Assist with sample management
Support in drug product development studies
Additional Skills & Qualifications
PhD with 1+ years, MS with 3+ year or BS with 5+ years’ experience in analytical development and quality control in pharma/biotech
· Experience with analytical techniques for protein analysis (., SDS-PAGE, SEC HPLC, CE-SDS, IcIEF, ELISA) is required; working knowledge of laboratory software (., Empower, Compass, SoftMax, AccuSEQ, SoloVPE) is highly preferred
understanding of veeva vault quality systems
Job Type & Location
This is a Contract position based out of Lexington, MA.
Pay and BenefitsThe pay ran...
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