Specialist Iii, Qa (batch Disposition)

Seqirus

Holly Springs, North Carolina, US
Cgmp compliance
Batch documentation review
Product release
The QA Specialist supports review of batch documentation and release of internal and external commercial products, while ensuring compliance with cGMPs, site SOPs, and regulatory requirements

Job Summary

  • The QA Specialist supports review of batch documentation and release of internal and external commercial products, while ensuring compliance with cGMPs, site SOPs, and regulatory requirements.
  • Responsible for certification and/or rejection of incoming material, manufactured material, including intermediates, buffers, virus seed, monobulk and drug product in compliance with applicable licenses and legal requirements.
  • You Belong at CSL: Inclusion and Belonging is at the core of our mission and who we are.

Matching Summary

The QA Specialist supports review of batch documentation and release of internal and external commercial products, while ensuring compliance with cGMPs, site SOPs, and regulatory requirements.

Skills & Requirements

Must-have

  • cGMP compliance
  • batch documentation review
  • product release
  • regulatory requirements
  • stakeholder communication

Nice-to-have

  • collaboration
  • problem-solving
  • continuous improvement
  • regulatory inspection representation

Key Requirements

  • University degree in a relevant scientific discipline
  • 3+ years GMP experience
  • Knowledge of cGMP principles
  • Knowledge of FDA and EMA requirements

Work Rights

Not specified

Tailored Resume

Cover Letter