Responsible for review and/or approval of basic and technical documentation, drafting and reviewing internal Quality policies and procedures, performing product related activities, performing Quality audit functions, performing product release activities, identifying process and Quality System improvements, and acting as a QA liaison internally and externally for drug, biologics or vaccine products. Master’s degree in Project Management, Biology, Chemistry, or related biology/pharmaceutical/engineering field and three years of experience as a QA Analyst or related occupation in quality assurance OR Bachelor’s degree in Project Management, Biology, Chemistry, or related biology/pharmaceutical/engineering field and five of experience as a QA Analyst or related occupation in quality assurance.