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Apogeetherapeutics
Apogeetherapeutics

Associate Director, GMP Quality Assurance

qafull-timeRemote
SALARY
Not listed
WORK TYPE
remote
JOB TYPE
full-time
INDUSTRY
healthcare
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About the role

Role Summary

We are seeking a dynamic and results-driven Associate Director of GMP Quality Assurance (QA) to join our team. You will play a pivotal role in ensuring the quality, safety, and compliance of our biologics manufacturing processes and device development activities (pre-filled syringes, autoinjectors, etc.) This position will work closely with cross-functional teams to establish, maintain, and continually improve Apogee’s quality systems. You will support our mission to develop and deliver differentiated biologic therapies to patients in need.

Key Responsibilities

  • Assist QA Leadership with development and execution of planned QA audit schedules supporting GMP activities
  • Partner with Technical Operations with selection and ultimate oversight of drug substance / drug product contract development manufacturing organizations (CDMOs) in support of Phase 3 and process performance qualification (PPQ) activities
  • Independently performs assigned GMP audits
  • Partner effectively with Technical Operations and provide quality guidance in GMP data and documentation generated
  • Verify manufacturing and testing activities adhere to GMP regulations and guidelines and ensure a culture of continuous improvement
  • Timely management of batch record review and release to ensure continuous supply for clinical trials, and to guarantee the consistent production of high-quality products
  • Ensure manufacturing processes, facilities, and systems adhere to current GMP regulations, guidelines, and industry standards
  • Provide QA support of device development activities (pre-filled syringes, autoinjectors, etc.)
  • Maintain robust GMP quality systems, including documentation, change control, deviations, CAPA, and quality events
  • Maintain knowledge of current regulatory changes and industry trends and translate new requirements back to the company’s policies and procedures
  • Implement risk-based approaches to quality management, identifying and mitigating quality risks across the organization
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