Senior Research Scientist 2- Formulation

Julphar; Ras Al Khaimah; On-site; AED 30,000 - 50,000; Full time

Job summary

A pharmaceutical company in Ras al-Khaimah is seeking a Senior Research Scientist 2 to play a key role in the formulation development of pharmaceutical products for regulated markets. Responsibilities include conducting literature reviews, developing product profiles, and preparing regulatory documentation. The ideal candidate has 8+ years of formulation development experience, particularly with Biosimilars and Injectables.

Qualifications

• Minimum 8 years of hands-on experience in Formulation Development for regulated markets.
• Experience with regulatory agencies such as US-FDA, EU, Canada, UAE.
• Background in developing multiple dosage forms, particularly Biosimilars and Injectables.

Responsibilities

• Conduct literature surveys and patent searches.
• Develop Quality Target Product Profiles (QTPP).
• Compile product development reports.

Skills

Result and process orientation

Attention to detail

Team collaboration

Effective communication in English

Task management

Education

Master’s degree in Pharmacy

Bachelor’s degree in Pharmacy

Job description

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 and 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 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.

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