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Pharma Products Researcher / Regulatory Affairs – Qatar

Jobs for Humanity · Mumbai

New
Mid 🇬🇧 English
Regulatory submission software Data analysis tools

Job description

About the role

We are seeking a highly skilled Pharma Products Researcher / Regulatory Affairs specialist to join our team in Mumbai, India. This role will focus on conducting pharmaceutical research and managing regulatory affairs for our products in the Qatar market.

Key responsibilities

  • Conduct comprehensive research on pharmaceutical products, focusing on their suitability for the Qatar market.
  • Analyze and interpret scientific data to support product development and regulatory submissions.
  • Prepare and review regulatory documentation for submission to Qatar's health authorities.
  • Monitor and interpret changes in Qatar's pharmaceutical regulations and assess their impact on our products.
  • Collaborate with cross‑functional teams to ensure compliance with local and international regulatory requirements.
  • Develop and maintain relationships with key stakeholders, including regulatory agencies and industry partners.
  • Provide expert advice on regulatory strategies to support product development and market entry in Qatar.
  • Manage and track multiple regulatory projects, ensuring timely completion and adherence to quality standards.

Required profile

  • Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, or a related field.
  • Minimum 3‑5 years of experience in pharmaceutical research or regulatory affairs.
  • In‑depth knowledge of Qatar's pharmaceutical regulations and regulatory processes.
  • Strong understanding of international pharmaceutical regulations (FDA, EMA).
  • Proficiency in regulatory submission software and data analysis tools.
  • Excellent technical writing skills for clear, concise regulatory documents.
  • Strong analytical and problem‑solving abilities.
  • Ability to manage multiple projects simultaneously and meet deadlines.
  • Fluency in English; Arabic language skills are highly desirable.
  • Regulatory Affairs Certification (RAC) is preferred.
  • Willingness to travel to Qatar as required.

Required skills

  • Regulatory submission software
  • Data analysis tools
  • Scientific data analysis

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Source : ats:smartrecruiters

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Published 3 days ago

Expires 1 month from now

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