Cadila Pharma

JOB RESPONSIBILITIES
•To prepare, review and submit dossiers for Life cycle management, and other submissions as required for UK, EU regions.
•Preparation, review and submission of eCTD Renewal, variations, post marketing applications and other related activities.
 •Timely initiation and follow-ups with cross functions for necessary document support for preparation and submission of new/Query response etc. 
•Discuss project based with immediate supervisor for all submission/Query-response/Variations etc. for technical inputs during preparation & e-Submission within stipulated timeframe agreed.
•Regulatory review, technical support and submissions, as needed, for UK Site transfer projects.
•Preparation and submission of variation applications to support post approval changes, new OLS and site transfer projects for UK markets.
•Review and approve SAP orders and technical documents from cross functions related to registrations/submissions/variations related all submission related documents like CC, Spec/STPs, Protocols/reports, MMDs, Labelling/Art works etc.), as required.
•Prepare/update project trackers related to variations with defined action points and target timelines.
•Maintain appropriate archival of submission related documents.
•Regulatory support/inputs for contract manufacturing projects for UK, EU as directed.
•To attend and represent my supervisor in required technical meetings with main Cross functions for any variation related needs, as and when required.
•Take up for required technical support or additional activities as per business need on Supervisor instructions.
•Discuss with Supervisor with daily/regular updates on projects, any technical concern.

Job Details

Skills Required

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