Pharmaceutical Documentation Specialist Papillon Resource Management Private Limited

3.0 - 5.0 years

3 - 5 Lacs

Navi Mumbai

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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.

Posted 4 months ago

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Pharmaceutical Documentation Specialist Papillon Resource Management Private Limited

3.0 - 5.0 years

3 - 5 Lacs

Navi Mumbai

Work from Office

Posted 4 months ago

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Management Associate Ashkom

2.0 - 6.0 years

0 - 3 Lacs

Mumbai Suburban

Work from Office

Job Title: Management Associate MPD – AMA Contract Resource Department: MPD-BB, AMA PHC Location: Andheri East Chakala, Mumbai Position Type: Full-Time, Contractual Vacancies: 1 Job Description: We are seeking a Management Associate to support the MPD – AMA team on a contractual basis. This role involves key responsibilities in pharmaceutical documentation, data management, and coordination to ensure efficient support to formulation and analytical development teams. Key Responsibilities: Setup of Enovia DSM for formulation parts and documentation. Compilation and tracking of stability study data for review and approval in Enovia. Raise and manage Change Controls in Veeva QA system for MPD de...

Posted 5 months ago

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