Sr. Research Scientist 2

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