Summit, NJ

Responsibilities of the Quality Assurance Specialist, cGMP

Responsible for accurate and timely review and release of manufacturing batch records and other pertinent documents and records used at a manufacturing and testing facility in accordance with policies, standards, procedures and Global cGMPs
Reviews executed batch records for documentation completeness and accuracy
Obtains any identified GMP/GDP batch record corrections from manufacturing personnel
Communicates effectively with other departments within the organization and functions well within a team environment


Qualifications of Quality Assurance Specialist, cGMP

1+ years of experience working in a cGMP environment
Possesses strong interpersonal and time management skills, and the abilities to work well in a team environment and coordinate multiple tasks efficiently
Hands-on experience with batch record review and product disposition preferred
High school diploma required, bachelor's degree preferred


Compensation for the Quality Assurance Specialist, cGMP

Salary Range: Commensurate with experience
Benefits: Comprehensive; Medical, Dental, Vision, 401k, and PTO
Multiple shift times available