Pharma Products Researcher / Regulatory Affairs - Qatar

Jobs for Humanity • Arabic (Optional) • English: C1 • Pharmaceuticals • Travel required • Bachelor's Degree • 9 months ago
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Salary
≈ $11k – $25k per year (Estimated)
Location
In office (Mumbai)
Seniority
Intern · 3+ years exp
Employment
Full-Time
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Jobs for Humanity

Jobs for Humanity is a New York based non-profit recruiting organisation founded in 2020 that connects historically underrepresented candidates with employers committed to inclusive hiring. It works with refugees, people with disabilities, neurodivergent candidates, formerly incarcerated people, returning parents and older workers, running job boards, hiring events and coaching alongside advisory work that helps companies rewrite job descriptions and interview processes. The organisation aggregates and reposts a very large number of partner vacancies, which is why it appears as the poster of record on listings that belong to its client employers.
jobsforhumanity.com • HQ: New York, United States • Career Services • Event Management • Events & Ticketing • Job Boards & Aggregators • Recruiting & Staffing • Internet Services • Professional Services • 11-50 employees • Est. 2020

Aldibel L.L.C is dedicated to , ensuring top-notch services and products that cater to the unique needs of our clientele.

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. The successful candidate will play a crucial role in ensuring our products meet all regulatory requirements while supporting our research initiatives.

  • 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 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
  • 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 with the ability to prepare clear, concise regulatory documents
  • Strong analytical and problem-solving skills
  • Ability to manage multiple projects simultaneously and meet deadlines
  • Excellent communication and interpersonal skills
  • Fluency in English; Arabic language skills are highly desirable
  • Regulatory Affairs Certification (RAC) is preferred
  • Willingness to travel to Qatar as required
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