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Regulatory Affairs Consultant (Biologics/Small Molecules)

7 - 10 years

0 Lacs

bengaluru karnataka india

Posted:1 week ago| Platform: Linkedin logo

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Skills Required

management planning maintenance analysis strategy remediation reports evaluation controls documentation labeling content data

Work Mode

On-site

Job Type

Full Time

Job Description

  • Around 7-10 years of relevant experience in handling life cycle management of approved drug products (small molecules as well as biologicals including Vaccines, monoclonal antibodies) in various markets.
  • Good understanding of regulatory framework, including regional trends, for various types of applications and procedures.
  • Lead and / or contribute to the planning, preparation, authoring and delivery of regulatory maintenance submissions from either a global and/or regional perspective.
  • Responsible for managing (Authoring and Review) of biosimilar investigational product submission such as IND & IMPD for USFDA, EMA
  • Authoring, review, and submission of BLA/MAA of biosimilar dossiers for US/EU/ROW /India markets.
  • Preparation / Review of Regulatory gap analysis and strategy documents (with remediation plans for identified gaps) for submissions like IND, IMPD, DMF, BLA, NDA, and MAA applications.
  • Life cycle management (LCM) for approved products. (Annual reports, variations, renewals) for Europe (Type IA/IB/II/IAIN) / US and other ROW markets.
  • Evaluation of change controls and deviations and defining regulatory strategy .
  • Co-ordination with internal and external stake holders for documentation required for filing. Identify quality and/or timeliness issues with source documents, as early as possible
  • Develop up-to-date knowledge about regulatory guideline updates and applies regulatory requirements and their impact on submissions.
  • Working experience in Regulatory Information Management Systems like Veeva Vault.
  • Strong communications skills and ability to guide and mentor team members.
  • Ability to work independently.
  • Review and submit safety variations to Health Authorities and perform post Approval CMC / labeling related updates.
  • Authoring content of the label (EU, Canada, AU/NZ & US) based on Company Core Data Sheet (CCDS) / PRAC / CMDH recommendations.
  • Familiarity with EU Guidelines for QRD / Excipients.
  • Artwork management for countries with label in English.

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