Granules Pharmaceuticals
QA Associate, Quality Compliance (Generic Pharma)
Granules Pharmaceuticals, Chantilly, Virginia, United States, 22021
Job Type
Full-time
Description
This role is an exciting opportunity to be a part of the Quality Assurance team at Granules Pharmaceuticals, Inc. in Chantilly, VA. As a member of a growing team, you'll play an important role maintaining, tracking and closure of all Quality events.
Requirements
Key Responsibilities
Improve and maintain Quality Management System at site in line with current regulations, including change management, deviation and CAPA management. Responsible to adhere to data integrity requirements and ensure the same are implemented in Quality management Systems. Partner with cross-functional leads in timely initiation, implementation and closure of Quality Management System elements. Support in Implementation of TrackWise Digital at site. Responsible for initiation of Deviations, initial impact assessment and investigations relating to Quality Assurance functions. Participate in organization and execution of Internal Audit Program for site. Responsible for data analysis/trending, including escalation and development of action items as required. Additional duties as required. Minimum Skills & Qualifications
Bachelor's degree At least 2 years of QA experience in pharmaceutical or related industry Experience working with Quality Management Systems TrackWise experience preferred
Full-time
Description
This role is an exciting opportunity to be a part of the Quality Assurance team at Granules Pharmaceuticals, Inc. in Chantilly, VA. As a member of a growing team, you'll play an important role maintaining, tracking and closure of all Quality events.
Requirements
Key Responsibilities
Improve and maintain Quality Management System at site in line with current regulations, including change management, deviation and CAPA management. Responsible to adhere to data integrity requirements and ensure the same are implemented in Quality management Systems. Partner with cross-functional leads in timely initiation, implementation and closure of Quality Management System elements. Support in Implementation of TrackWise Digital at site. Responsible for initiation of Deviations, initial impact assessment and investigations relating to Quality Assurance functions. Participate in organization and execution of Internal Audit Program for site. Responsible for data analysis/trending, including escalation and development of action items as required. Additional duties as required. Minimum Skills & Qualifications
Bachelor's degree At least 2 years of QA experience in pharmaceutical or related industry Experience working with Quality Management Systems TrackWise experience preferred