Roles And Responsibilities: Review data generated in the laboratory is accordance with stablished criteria set forth in SOPs and established specifications
Assemble quality data to support management review meeting requirements
Issuing, reviewing, maintaining, and archiving of laboratory logbooks
Scanning of laboratory approved finalized qualification for easy accessibility by all department
Training and execution of internal audits, as required
Review/approval of calibration records for analytical instrumentation and equipment
Identify and report any non-conformances and/or discrepancies to management if applicable.
Complete other duties or participate in project work as assigned by management.
Education and Experience
Minimum bachelor’s degree from an accredited college/university in relevant field of study such as Chemistry, Pharmaceutical Science, or other Life Science discipline.
Advanced training or education in pharmaceutical quality compliance or related field of study from an accredited college/university.is preferred.
Minimum of 1 year of experience in quality assurance in a current Good Manufacturing Practice (cGMP)