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Deputy Manager
Cadila Pharmaceuticals Ltd
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Posted: 27 Sep 26
Job Description
Principal Tasks & Responsibilities
New & Renewal Dossier Filings: Prepares, reviews, and submits new and renewal registration dossiers to support SBU targets across specified countries.
MoH & Customer Query Resolution: Drafts and shares pre-registration responses to customer and Ministry of Health (MoH) queries within stipulated timelines.
Technical Document Review: Approves critical regulatory documents including Change Controls, specifications, stability protocols, MMD II, and artwork for compliance.
Post-Approval Life Cycle Management: Updates dossiers and files variations for post-approval changes to maintain ongoing market compliance.
SAP Order Approval: Reviews and approves SAP orders for specified international markets across all customer accounts.
Cross-Functional Coordination: Partners with R&D, QA, QC, Marketing, and Purchase to streamline filing timelines, tender submissions, and query responses.
Database & Project Tracking: Maintains registration databases and updates project trackers for approved products, ongoing filings, and active queries.
Team Guidance & Compliance: Educates team members on changing registration guidelines, project updates, and unplanned SBU priorities..
Key Skills & Competencies
Functional / Technical:
Preparation, review and submission of new as well as renewal dossiers
Response to customer and respective MoH queries
Maintain appropriate database for registration
Behavioural:
Result Orientation – Level 4
Process Orientation – Level 4
Team Work & Collaboration – Level 4
Job Particulars
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2952769
Job Category Regulatory Affairs
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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