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

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 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 visit www.Julphar.net to read more about us and the journey of Julphar