Life cycle management of the Drug Master Files (Amendments, Annual Reports, CEP updates and Bi-Annual updates). Preparation, review and submission of Applicant's Part DMF (Open Part DMF) and Technical data package to customers. Handling of DMF deficiencies received from regulatory agencies
Position will be responsible for Spreading IGF (Idea Generation Form) circulation to all stakeholders PD, AD, RA, CQA,F&A, IP, Packaging, SC & Plant and seek their opinion Managing project initiation functions during pre-DIF (Development Initiation form) stage, Project code assignment in ERP ...
We have following urgent openings for our CQA team: 1. CQA (Audits, Validation, QMS) - Male Candidates Prefered. Required: B.Pharma / M.Pharma / MSc with 4-8 years of same CQA experience in Validation, QMS, Regulatory Audits etc. 2. CQA (Market Complaints review & Investigation, Packaging
Handling Pharma & Food Sales distribution,Strategic Planning Business Development,Sales & Marketing,Product Promotion, Business 2 Business Sales,Distribution/Channel Management,Client Relationship Management Man Management,Project Management