Associate Director – Process Technical Lead For Drug Product Aseptic Manufacturing

AstraZeneca

Singapore
**
Aseptic filling and lyophilization expertise
Process design and scale-up
Technology transfer leadership
** AstraZeneca is seeking an Associate Director – Process Technical Lead for Drug Product Aseptic Manufacturing at their new biologics manufacturing campus in Singapore. The role involves providing technical leadership in aseptic manufacturing processes, technology transfer, and regulatory compliance, while contributing to a significant investment aimed at advancing life-changing medicines. **

Job Summary

  • Be part of history in the making at AstraZeneca's first biologics manufacturing campus in Singapore, a groundbreaking USD 1.5 billion investment serving as a global hub for innovation and excellence.
  • Provide technical leadership for Drug Product Aseptic Manufacturing, defining CQAs and CPPs, engineering control strategies, and partnering across multiple teams for process design, scale-up, and technology transfer.
  • Join a team that combines rigor with curiosity, working with modern manufacturing technologies and digital tools to advance life-changing medicines for patients everywhere.

Matching Summary

Match Score: 75

** AstraZeneca is seeking an Associate Director – Process Technical Lead for Drug Product Aseptic Manufacturing at their new biologics manufacturing campus in Singapore. The role involves providing technical leadership in aseptic manufacturing processes, technology transfer, and regulatory compliance, while contributing to a significant investment aimed at advancing life-changing medicines. **

Skills & Requirements

Must-have

  • Aseptic filling and lyophilization expertise
  • Process design and scale-up
  • Technology transfer leadership
  • Troubleshooting and deviation management
  • Regulatory dossier authoring
  • Advanced analytics and digital tools

Nice-to-have

  • Bold thinking and innovation
  • Drive for sustainability
  • Lean thinking and execution
  • Kindness alongside ambition

Key Requirements

  • 7-10+ years in biopharma MSAT/Process Engineering/Validation
  • Direct leadership in Drug Product manufacturing
  • Experience in aseptic filling and lyophilization
  • Proven track record in technology transfers
  • Facility lifecycle experience (Design, qualification, validation)
  • Ability to drive cGMP compliance

Work Rights

Not specified

Tailored Resume

Cover Letter