Free · takes a minute · your resume fills your profile
CoreHRx never asks candidates for money. If anyone does, .
Role at a glance
You will
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
Experience
3–5 years
Education
Bachelor's degree
Must-have skills
Data Analysis
How well do your skills match this job?
Sign in to see your fit: the skills, experience and location this job asks for, checked against your profile.
Job description
Location: Mumbai, MH, India Department: Health Care Provider
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
Company Description
Aldibel L.L.C is dedicated to , ensuring top-notch services and products that cater to the unique needs of our clientele.
