QC Analyst III

About the role

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-compliant Quality Control laboratory.

Responsibilities

• Independently write experiment summaries, laboratory investigations, technical reports, operation and test method procedure documents.
• Review and approve CCRs according to the change control process.
• Provide analytical support for formulation development.

Requirements

• Master’s degree (or foreign equivalent degree) in Chemistry, Analytical Chemistry, or related field.
• 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.

Qualifications

Not specified.

Skills

• Preparing validation protocols and reports.
• Preparing test methods and procedures.
• Reviewing and approving CCRs according to the change control process.
• Providing analytical support for formulation development.

Benefits

Not specified.

Pay

$103,000 per year.

Schedule

Not specified.