Job Overview
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Date PostedJuly 19, 2023
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Location (State / UT)
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Expiration dateFebruary 27, 2026
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Experience3 Years, 8 Years
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GenderAny
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Desired QualificationBachelor Degree, Master’s Degree
Job Description
Process Incharge/Sr Process Incharge – Regulatory Affairs (ROW)
Roles and Responsibilities:
- Dossier preparation/review as per the country-specific guideline/CTD guideline
- Timely query response submission to Distributor/ MOH
- Review of documents for their correctness and compliance with respective regulatory guidelines (as per country requirement)
- Preparation, review & release of artworks & sales orders as per country approval
- Variation documents preparation and filing as per country requirements
- Timely dispatch of tender documents to country/parties as per the deadline
Desired Candidate Profile:
- Should be able to review & interpret the requirement as per country-specific/ tender guideline
- Should be able to review various plant documents for dossier preparation like Process validation, Stability study, PDR, Method validation, SOP, Drug Master file, BMR, APR, etc.
- Should be able to handle a team of two members
- Should be able to communicate with relevant functions for procurement of required regulatory documents
- Should be able to communicate with relevant counterpart at country
- Preferred Immediate joiners
Qualification: B Pharma, M. Pharma
Experience: 3 – 8 years
Perks and benefits: 5 Days working & other benefits