3 - 5 years
3 - 5 Lacs
Posted:1 week ago|
Platform:
Work from Office
Full Time
Develop and manage comprehensive pharmaceutical-grade documentation throughout the project lifecycle.Prepare key qualification documents: Design Qualification (DQ), Functional Design Specification (FDS), Hardware Design Specification (HDS). Required Candidate profile • 3-5 years of experience specifically in pharmaceutical documentation or a similar quality/validation role within a regulated industry. • Strong understanding and practical experience with DQ,FDS,HDS
Papillon Resource Management Private Limited
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