Candidate should be well versed with the regulatory guidelines. Candidate should have shop floor experience of In-process control involving Non sterile and sterile operations.
B.Pharm / M. SC in Chemistry / Biotechnology; Experience into Media Fill Activities Exposure into EM Monitoring as QA Knowledge about Sterility, MLT, BET, Water Analysis, Media Preparation; Analysis of Raw Material / Finished product / Intermediates / Stability / Instrumentation / Sampling
Sun Pharma is the fourth largest specialty generic pharmaceutical company in the world. We provide high- quality, affordable medicines trusted by healthcare professionals and patients in over 150 countries.
Discuss base forecast and bottom up forecasts with sales & marketing team and develop consensus forecast. Upload consensus forecast in system and share with Supply Planning Team
Review of all the documents received from stake holder for dossier compilation , Query response and Life cycle management. Allocation of projects to regulatory associate & manage the team for all the regulatory submission activities
To ensure that the products are manufactured and stored as per appropriate documents in order to obtain the required quality. To ensure that the production records are reviewed as per current procedures.
Review all data and documents related to product registrations for various health authorities. Compile registration dossiers for submission to various health authorities like – US, Canada, Europe, Australia