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.Roles and ResponsibilitiesConduct literature surveys, patent searches, and prepare Prototype Formulation Reports.Identify reference products and initiate procurement processes.Develop Quality Target Product Profiles (QTPP) based on literature insights and reference product characterization.Development of Injectable dosage forms; Biologics/Biosimilar products- upstream & downstream, for regulated markets.Identify and finalize API and excipient sources for new product development.Perform and conclude pre‑formulation and drug–excipient compatibility studies for assigned projects.Contribute to product process optimization and reformulation activities, including report preparation and closure.Prepare registration dossiers for submission and support CTD/dossier documentation requirements.Plan, design, and execute pharmaceutical experiments using the QbD (Quality by Design) approach.Review analytical development data and systematically compile product‑related data.Support manufacturing of batches for process optimization, submission, and bioequivalence (BE) studies.Assist in pilot and scale‑up batch manufacturing, with necessary documentation, and facilitate technology transfer to production.Develop and maintain R&D‑related SOPs in compliance with cGMP and GDP principles.Prepare and submit periodic project reports to management.Collaborate cross‑functionally with Analytical R&D, Supply Chain, Production, QC, QA, Regulatory Affairs, and Medical Affairs to ensure timely project completion.Handle Technology Transfer out/Contract Manufacturing activities for assigned projects.Experience in packaging development and life cycle management.Qualification/Functional KnowledgeEducation: Master’s degree in Pharmacy/ Master’s degree in BiotechnologyExperience:Minimum 8 years of extensive experience of working in Formulation Development of Injectable dosage forms; Biologics/Biosimilar products- upstream & downstream, for regulated markets.Significant exposure in addressing regulatory queries for US‑FDA, EU, Canada, UAE, KSA and other stringent regulatory markets.Past experience of handling different dosage forms in R&D i.e. injectables, Biosimilars, Biologics etc.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#J-18808-Ljbffr