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 deviations, CAPA, change controls, and investigations.
Assist in preparatio...
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 deviations, CAPA, change controls, and investigations.
Assist in preparatio...
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