The role involves ensuring product conformity to national and international pharmaceutical regulations through rigorous quality assurance processes
Job Summary
The role involves ensuring product conformity to national and international pharmaceutical regulations through rigorous quality assurance processes.
Candidates will be responsible for approving production documentation, managing critical master data, and coordinating with global teams on data integrity.
This position serves as a Quality Subject Matter Expert for equipment qualification using the Critical Aspect Risk Assessment approach.
Matching Summary
The role involves ensuring product conformity to national and international pharmaceutical regulations through rigorous quality assurance processes.
Skills & Requirements
Must-have
Master Batch Record approval
GMP compliance verification
Critical data management
Change control processes
Risk assessment (CARA)
System qualification oversight
Nice-to-have
CSV knowledge preferred
Cross-functional collaboration
Subject Matter Expertise in Data Integrity
Project team leadership
English language proficiency
Key Requirements
Master's degree in Chemistry, Pharmacy, Biology, Engineering, or IT