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August Bioservices

US-based CDMO for end-to-end drug development

Associate Quality Engineer

Regulatory & Quality (Life Sciences)Posted on Nov 10
Full-timeNashville, TN, USANo salary listedIn-person

About the Job

Requirements

  • 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

Responsibilities

  • Support quality activities for new product onboarding, technology transfer, and project initiation efforts
  • Collaborate with Quality Engineers to draft and revise quality documentation including stability protocols and reports
  • Collaborate with Quality Engineers to draft and revise finished good product specifications
  • Collaborate with Quality Engineers to draft and revise 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.
  • 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

About the Company

August Bioservices

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.

Company size
51-200
Company stage
Series B
Total funding
$88.6M
Headquarters
Nashville, TN
Founded
2017

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