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Posted 4 months ago

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Regulatory Affairs Post-Approval Associate-Europe - DEMO Global Services Center

HyderabadOn-siteFull-time

AI Summary

A Regulatory Affairs Associate handles post-approval regulatory submissions, variations, and compliance for EU and global markets for sterile, non-sterile, and oral solid/liquid pharmaceutical products.

About this role

At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Associate to join our team. The job responsibilities for this position includes post-marketing regulatory submissions for Europe and other global markets for sterile, non-sterile and oral solid/liquid products. This position is based at ** Hyderabad, India.**

Responsibilities:

  • Understanding of Regulatory strategy and documentation requirements for EU variations including renewals, extensions for Sterile (SVP, LVP, lyophilized, ophthalmic etc.), non-sterile and oral solid/liquid products.
  • Collect, prepare, compile regulatory documentation, for the product’s lifecycle maintenance (administrative, quality, safety variations and renewal procedures).
  • Prepare and coordinate responses to Deficiency Letters (DLs) and other CMC-related regulatory queries in collaboration with cross-functional teams
  • Preparation of module 1 documentation for as per assigned timelines for out-licensing and in-licensing products in EU countries
  • Liaise with various departments to collect all necessary information and documentation, in accordance with defined guidelines for Pharmaceutical Dossier submission and product registration
  • Liaise with external Regulatory authorities as required
  • Act as responsible Regulatory Team member for assigned regulatory projects
  • Support internal activities of Regulatory department in order to ensure regulatory compliance of registered products

Requirements

  • Bachelor or Master Degree in Pharmacy with 3+ years of experience in Regulatory Affairs / CMC within a Pharmaceutical organization.
  • Knowledge of CMC and global regulatory guidelines for Sterile (small & large volume parenteral, aqueous solution, lyophilized product, sterile powder etc) and oral solid/liquid dosage form.
  • Strong organization skills, multi-tasking and able to meet deadlines.
  • Effective communication and relationship management.
  • Ability to work under pressure, resilience.

Benefits

The company offers competitive salary and benefits, continuous specialized training, career development and a friendly working environment.

Skills

CMCEU Regulatory VariationsEU Renewals And ExtensionsNon-sterile ProductsOral Solid/liquid ProductsPharmaceutical Regulatory AffairsRegulatory Documentation And DossiersSterile Products (SVP, LVP, Lyophilized, Ophthalmic)

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