QC Associate Scientist

RESPONSIBILITIES:

• Providing Quality Review/Oversight of site GMP documentation related to the operation of a vaccine manufacturing facility to ensure compliance

• Performs testing including, but not limited to clinical and/or commercial product, raw materials and validation samples.

• Analyzes and interprets results, makes decisions regarding the accuracy, completeness and compliance.

• Responsible for final authorization/approval/release of documentation/equipment/processes

• Assessing existing situations and suggesting improvements in the Quality systems to increase compliance throughout the facility

• Plans projects and may initiate and develop plans to ensure their timely completion