Associate Quality Engineer
August Bioservices
Associate Quality Engineer
August Bioservices
US-based CDMO for end-to-end drug development
The Associate Quality Engineer supports quality activities related to the introduction of new products and projects into the quality system. This role works closely with Quality Engineers to assist with documentation development, project coordination, and quality system execution during new product onboarding.
In addition, the Associate Quality Engineer supports the Senior Quality Engineer by facilitating and coordinating meetings and documentation related to deviations and investigations. This position is ideal for a recent graduate or early-career professional seeking hands-on experience in pharmaceutical quality engineering and regulated environments.
New Product Onboarding & Documentation Support
Support quality activities for new product onboarding, technology transfer, and project initiation efforts
Collaborate with Quality Engineers to draft and revise quality documentation including, but not limited to:
Stability protocols and reports
Finished good product specifications
Quality plans and project-specific quality documentation
Assist with document formatting, routing, review coordination, and approval workflows in document control systems
Support tracking of project onboarding deliverables, milestones, and quality-related action items
Work collaboratively with clients and internal cross-functional stakeholders to move projects forward.
Deviation & Investigation Coordination Support
Support the Senior Quality Engineer by coordinating and facilitating meetings related to deviations, investigations, and CAPA activities
Assist with document assembly and data gathering to support investigation records
Support timely communication between cross-functional stakeholders involved in investigations
Bachelor’s degree in chemistry, biology, or a related technical discipline with 2-3 years of pharma experience OR an advanced degree in chemistry, biology, or a related technical discipline with 1-2 years of pharma experience (or other regulated manufacturing setting)
Basic understanding of pharmaceutical or regulated manufacturing environments
Strong attention to detail and organizational skills
US-based CDMO for end-to-end drug development
August Bioservices is a US-based CDMO that provides end-to-end drug development and manufacturing from preclinical to commercial stages. It manages all steps in a single program, including research, development, testing, laboratory services, and sterile fill/finish, while following cGMP standards. It differentiates itself with a hybrid model that combines large-CDMO scale and capabilities with a strong focus on customer service and integrated workflows. Its goal is to help clients bring safe and effective drugs to market efficiently by delivering comprehensive development and manufacturing under one roof.
Explore more opportunities at August Bioservices