1 Pharmaceutical Research jobs in the United Arab Emirates
Research Scientist - Pharmaceutical Formulations
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Job Description
Join a team of innovative researchers in formulation development and play a key role in creating cutting-edge pharmaceutical products for regulated markets.
About the RoleThis exciting position involves hands-on research and development activities, cross-functional collaboration, and end-to-end project management from literature review to technology transfer. The successful candidate will work closely with various departments to ensure project timelines are met and deliver high-quality results.
Responsibilities- Conduct comprehensive literature surveys and patent searches to identify best practices and emerging trends.
- Develop Quality Target Product Profiles (QTPP) based on literature and reference product characterization, ensuring compliance with regulatory requirements.
- Finalize API and excipient sources for new product development, considering cost-effectiveness and supply chain reliability.
- Execute pre-formulation studies and drug-excipient compatibility assessments to optimize product performance.
- Drive process optimization and reformulation activities, documenting all changes and closures thoroughly.
- Prepare regulatory dossiers and support CTD documentation for submissions, working closely with regulatory affairs teams.
- Design and execute pharmaceutical experiments using Quality by Design (QbD) principles, ensuring data integrity and accuracy.
- Review analytical development data and compile comprehensive product development reports, highlighting key findings and recommendations.
- Support batch manufacturing for process optimization, regulatory submissions, and bioequivalence (BE) studies, collaborating with production teams.
- Assist with pilot and scale-up batches, including documentation and technology transfer to production, ensuring seamless execution.
- Develop and maintain R&D Standard Operating Procedures (SOPs) aligned with current Good Manufacturing Practice (cGMP) and Good Distribution Practice (GDP) standards.
- Submit periodic project reports to management for review and alignment, providing progress updates and key metrics.
- Collaborate with various departments, including Analytical R&D, Supply Chain, Production, QC, QA, Regulatory Affairs, and Medical Affairs, to ensure project success.
- A Master's degree in Pharmacy or a related field is preferred, but a Bachelor's degree in Pharmacy with relevant experience may also be considered.
- A minimum of 8 years of hands-on experience in Formulation Development for regulated markets, with a proven track record of addressing regulatory queries and inquiries.
- Strong background in developing and handling multiple dosage forms, particularly Biosimilars and Injectables, with expertise in Technology Transfer and Contract Manufacturing processes.
We value diversity and inclusion, and welcome applications from talented individuals who share our commitment to excellence and innovation. Apply today and join our dynamic team of researchers and scientists!
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