Preparation of regulatory dossiers in eCTD format for Europe (hands-on experience in eCTD is a must).
Thorough understanding and working knowledge of EU regulatory procedures including DCP (Decentralized Procedure) and MRP (Mutual Recognition Procedure).
Compilation and submission of regulatory dossiers for ROW (Rest of the World) markets.
Coordination and preparation of responses to deficiencies/queries received from Regulatory Agencies.
Application of ICH and EU regulatory guidelines during dossier preparation and submission.
Preparation and submission of variation packages for approved products in compliance with applicable regulations.
Desired Profile:
Bachelors/Masters degree in Pharmacy or Life Sciences.
25 years of relevant experience in Regulatory Affairs with proven expertise in eCTD dossier preparation.
Good knowledge of EU regulatory environment and ROW regulatory requirements.
Strong analytical, documentation, and communication skills.
Ability to work independently as well as in cross-functional teams.
Job Classification
Industry: Pharmaceutical & Life SciencesFunctional Area / Department: Legal & RegulatoryRole Category: Corporate AffairsRole: Regulatory Affairs ComplianceEmployement Type: Full time