GMP QA Analyst: Compliance, Doc Review & Release

ALLTECH CONSULTING SVC INC; Winchester (KY); On-site; USD 55,000 - 75,000; Full time

Job summary

A leading consulting service provider is seeking a QA Associate in Winchester, Kentucky. The candidate must be knowledgeable in GMP regulations and capable of independently evaluating compliance of analytical documentation. Responsibilities include reviewing analytical release and stability data and approving controlled documents with minimal supervision. A BS in science (preferably Chemistry or Biochemistry) and a minimum of 3 years of related industry experience are required.

Qualifications

• Minimum of 3 years of applicable GMP industry experience.
• Experience in analytical laboratory, QC laboratory, Manufacturing, or QA is preferred.

Responsibilities

• Review of analytical release and stability data with minimal supervision.
• Review and approval of controlled documents such as protocols and test methods.

Skills

Critical thinking

Organizational skills

Professional communication

Education

BS science degree, preferably in Chemistry or Biochemistry

Job description

A leading consulting service provider is seeking a QA Associate in Winchester, Kentucky. The candidate must be knowledgeable in GMP regulations and capable of independently evaluating compliance of analytical documentation. Responsibilities include reviewing analytical release and stability data and approving controlled documents with minimal supervision. A BS in science (preferably Chemistry or Biochemistry) and a minimum of 3 years of related industry experience are required.