Pharma Products Researcher / Regulatory Affairs - Qatar
Jobs for Humanity · Mumbai
Data & AIFull-time
Jobs for Humanity is hiring a Pharma Products Researcher / Regulatory Affairs - Qatar in Mumbai, Maharashtra (full-time). Posted 31 December 2025. Apply directly on Jobs for Humanity's own careers site — no account needed.
Company Description
Aldibel L.L.C is dedicated to , ensuring top-notch services and products that cater to the unique needs of our clientele.
Job Description
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
Qualifications
- 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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