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.

Key Responsibilities:

Conduct comprehensive

literature reviews and patent searches

, and prepare

Prototype Formulation Reports

. Identify

reference products

and initiate

procurement processes

. Develop

Quality Target Product Profiles (QTPP)

through in-depth literature research and reference product characterization. Finalize

API and excipient sources

for new product development. Conduct

pre-formulation studies

and

drug-excipient compatibility

assessments for assigned formulations. Contribute to

formulation optimization and reformulation

activities; prepare reports and ensure timely project closure. Assist in the preparation of

registration dossiers

and support

CTD/dossier documentation

for regulatory submissions. Plan, design, and execute experiments using the

Quality by Design (QbD)

approach. Review

analytical development data

and systematically compile relevant formulation information. Support

manufacturing of batches

for process optimization, submission, and

bioequivalence (BE) studies

. Participate in

pilot and scale-up batch manufacturing

and facilitate

technology transfer

to production with appropriate documentation. Develop and maintain

R&D SOPs

in accordance with

cGMP and GDP

guidelines. Prepare and submit

project progress reports

to management on a periodic basis. Collaborate with cross-functional teams including

Analytical R&D, Supply Chain, Production, QC, QA, Regulatory Affairs, and Medical Affairs

to ensure timely project delivery. Oversee

technology transfer

and

contract manufacturing activities

for assigned projects. Participate in

packaging development

activities, ensuring compatibility and regulatory compliance. Handle

eQMS activities

, ensuring timely documentation, closure of actions, and adherence to quality systems.

Core Competencies:

Strong

result and process orientation

to support departmental goals. High sense of

ownership, accountability

, and attention to detail. Proactive,

cost-conscious approach

in decision-making. Demonstrated ability in

team leadership

, effective

task and time management

. Excellent

written and verbal communication

in English. Highly

organized, disciplined

, and self-driven.

Education & Qualifications:

Master's Degree in Pharmacy

or

Bachelor's Degree

with relevant formulation experience.

Experience Requirements:

Minimum

8 years

of extensive experience in

formulation development

for

regulated markets

. Proven expertise in handling

regulatory queries

for

US-FDA, EU, Canada, UAE, Jordan

, and

KSA

. Practical experience with a wide range of

dosage forms

including

solid, liquid, semi-solid

, and

injectable formulations

.
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