QC Analyst III

Kashiv Biosciences • Piscataway, NJ

2d • Onsite

About The Position

Be primarily responsible for the execution and review of HPLC/UPLC assays & impurity testing along with Bio-assays for release & stability purposes in a GMP-complaint Quality Control laboratory; independently write experiment summaries, laboratory investigations, technical reports, operation and test method procedure documents, and review documents comprising, but not limited standard operating procedures, standard test methods, validation protocols and reports.

Requirements

• Master’s degree (or foreign equivalent degree) in Chemistry, Analytical Chemistry, or related
• Knowledge of preparing validation protocols and reports
• Knowledge of preparing test methods and procedures
• Knowledge of reviewing and approving CCRs according to the change control process
• Knowledge of providing analytical support for formulation development

Responsibilities

• Execution and review of HPLC/UPLC assays & impurity testing
• Execution and review of Bio-assays for release & stability purposes in a GMP-complaint Quality Control laboratory
• Independently write experiment summaries, laboratory investigations, technical reports, operation and test method procedure documents
• Review documents comprising, but not limited to standard operating procedures, standard test methods, validation protocols and reports

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level