Qureos

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Regulatory Executive

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Key Responsibilities:

  • Prepare, review and compile regulatory submission dossiers for new product registrations and renewals.
  • Ensure compliance with national drug regulatory authority guidelines, packaging & labelling requirements, and pharma regulations.
  • Maintain regulatory filings, track regulatory changes and proactively update internal teams on implications.
  • Liaise with QA/RA, production, marketing and external regulatory agents/distributors as required.
  • Support post-approval changes, variations, and ensure documentation is maintained and audit-ready.

Requirements:

  • Pharm-D from a recognized institution.
  • 2–5 years’ experience in regulatory affairs or business development in the pharmaceutical industry.
  • Good understanding of regulatory submission formats (ACTD/CTD preferred) and life-cycle management.
  • Strong organizational, analytical and communication skills; able to work with cross-functional teams.
  • Proficient in MS Office (Word, Excel, PowerPoint) and able to maintain regulatory databases/tracking systems.

Job Type: Full-time

Application Question(s):

  • Please mention your current monthly salary.
  • What is your expected monthly salary for this position?
  • How many years of relevant work experience do you have in related field?
  • Where are you currently residing (city and area)?
  • If selected, how soon can you join?

Work Location: In person

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