Job Description

Step into a role where quality is not a checklist — it is a promise to patients waiting for life-changing therapies.

We are building a next-generation manufacturing ecosystem focused on advanced biologics and viral vector platforms. This role offers the opportunity to work at the intersection of science, compliance, and innovation while shaping a robust Quality Management System aligned with global regulatory expectations.

If precision excites you and documentation feels like architecture rather than paperwork — you will thrive here.

Key Responsibilities

  • Support the implementation and maintenance of the Quality Management System (QMS) in compliance with GMP and regulatory standards.
  • Manage the lifecycle of controlled documents including SOPs, specifications, protocols, and batch records.
  • Perform document review to ensure accuracy, completeness, and data integrity.
  • Participate in handling deviati...

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