Senior Research Scientist 1- Formulation

Julphar; United Arab Emirates; On-site; AED 120,000 - 200,000; Full time

Job summary

A leading pharmaceutical company in the UAE seeks a Senior Research Scientist 2 to drive formulation development for regulated markets. Responsibilities include literature surveys, developing Quality Target Product Profiles, and ensuring compliance with regulatory standards. Candidates should have 8+ years of experience, strong communication skills, and the ability to manage cross-functional projects.

Qualifications

• 8+ years of hands-on experience in formulation development for regulated markets.
• Experience addressing regulatory queries for US-FDA, EU, Canada, UAE.
• Strong background in developing biosimilars and injectables.

Responsibilities

• Conduct literature surveys and patent searches.
• Develop Quality Target Product Profiles based on reference products.
• Prepare regulatory dossiers for submissions.

Skills

Result and process orientation

Accountability and attention to detail

Team collaboration

Written and verbal communication in English

Cost-consciousness in R&D

Education

Master's degree in Pharmacy

Job description

At Julphar, we are on a journey of culture transformation & our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism.

Our core values: Respect, Collaboration, innovation, Integrity and Compassion - Combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable Talents , create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.

Job Overview

The Senior Research Scientist 2 will play a key role in the formulation development of pharmaceutical products for regulated markets. This position involves hands‑on R&D activities, cross‑functional collaboration, and end‑to‑end project management from literature review to technology transfer.

Key Responsibilities

• Conduct comprehensive literature surveys and patent searches; prepare Prototype Formulation Reports.

• Identify reference products and coordinate procurement activities.

• Develop Quality Target Product Profiles (QTPP) based on literature and reference product characterization.

• Finalize API andb>excipient sources for new product development.

• Execute pre‑formulation studies and drug–excipient compatibility assessments.

• Drive process optimization and reformulation activities with thorough documentation and closure.

• Prepare regulatory dossiers and support CTD documentation for submissions.

• Design and execute pharmaceutical experiments using Quality by Design (QbD) principles.

• Review analytical development data and compile comprehensive product development reports.

• Support batch manufacturing for process optimization, regulatory submissions, and bioequivalence (BE) studies.

• Assist with pilot and scale‑up batches, including documentation and technology transfer to production.

• Develop and maintain R&D SOPs in line with cGMP and GDP standards.

• Submit periodic project reports to management for review and alignment.

• Collaborate with departments including Analytical R&D, Supply Chain, Production, QC, QA, Regulatory Affairs, and Medical Affairs to ensure project timelines are met.

• Handle Technology Transfer Out and Contract Manufacturing for assigned projects.

• Oversee and manage eQMS activities related to R&D.

Core Competencies

• Strong result and process orientation with a proactive, responsible approach.

• High level of accountability, ownership, and attention to detail.

• Demonstrated cost‑consciousness in R&D operations.

• Effective team collaboration, time, and task management.

• Excellent written and verbal communication in English.

• Highly disciplined, motivated, and organized.

Educational Qualifications

• Master's degree in Pharmacy (preferred) or Bachelor's degree in Pharmacy.

Experience & Functional Knowledge

• Minimum 8 years of hands‑on experience in Formulation Development for regulated markets.

• Proven experience in addressing regulatory queries for agencies such as US‑FDA, EU, Canada, UAE, Jordan, and KSA.

• Strong background in developing and handling multiple dosage forms, particularly Biosimilars and Injectables.

• Expertise in Technology Transfer and Contract Manufacturing processes.

We value people from different backgrounds. Could this be your story? Apply today or visitwww.Julphar.netto read more about us and the journey of Julphar