Hengrui Pharma
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Job Responsibilities: 1.Lead feasibility assessment, dosage form design, formulation screening, process development, and optimization for 505(b)(2) NDAs and first-in-class innovative drugs. 2.Track clinical needs in key therapeutic areas to drive formulation innovations achieving enhanced efficacy/reduced toxicity. 3.Monitor global innovations in clinical-stage modified-release drugs; translate novel technologies/research concepts into R&D strategies. 4.Deepen expertise in formulation science while integrating cross-disciplinary knowledge (clinical pharmacology, medicinal chemistry, biopharmaceutics) for clinically driven drug development. 5.Establish in vitro-in vivo correlations (IVIVC) by analyzing pharmaceutical data and PK studies to link formulation properties with clinical outcomes. 6.Document experimental records; author regulatory submission documents ensuring data integrity and ALCOA+ compliance. 7.Execute assigned tasks: due diligence for in-licensed projects, novel technology platform assessments, literature reviews, e-journal editing, and technical training. Qualifications: 1.Ph.D. in Pharmaceutics, Pharmaceutical Sciences, or related field. Preferred: Experience with complex dosage forms (e.g., complex injectables, modified-release oral systems, inhalation products). 2.Comprehensive expertise in drug development with advanced technical proficiency; demonstrated ability to design scientifically sound studies and solve complex formulation challenges. 3.Proficient in literature mining (English journals/patents) with strong capability to extract, synthesize, and implement technical insights. 4.Intellectual curiosity and self-driven learning agility; embraces innovative/high-challenge tasks. 5.Hands-on experience with:Formulation equipment (e.g., fluid bed dryers, hot-melt extruders)DoE-based formulation screeningTechnical report writing. 6.Strong ethics, resilience in fast-paced environments, and collaborative mindset with excellent cross-functional communication skills.
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Job Responsibilities: 1.Lead feasibility assessment, dosage form design, formulation screening, process development, and optimization for 505(b)(2) NDAs and first-in-class innovative drugs. 2.Track clinical needs in key therapeutic areas to drive formulation innovations achieving enhanced efficacy/reduced toxicity. 3.Monitor global innovations in clinical-stage modified-release drugs; translate novel technologies/research concepts into R&D strategies. 4.Deepen expertise in formulation science while integrating cross-disciplinary knowledge (clinical pharmacology, medicinal chemistry, biopharmaceutics) for clinically driven drug development. 5.Establish in vitro-in vivo correlations (IVIVC) by analyzing pharmaceutical data and PK studies to link formulation properties with clinical outcomes. 6.Document experimental records; author regulatory submission documents ensuring data integrity and ALCOA+ compliance. 7.Execute assigned tasks: due diligence for in-licensed projects, novel technology platform assessments, literature reviews, e-journal editing, and technical training. Qualifications: 1.Ph.D. in Pharmaceutics, Pharmaceutical Sciences, or related field. Preferred: Experience with complex dosage forms (e.g., complex injectables, modified-release oral systems, inhalation products). 2.Comprehensive expertise in drug development with advanced technical proficiency; demonstrated ability to design scientifically sound studies and solve complex formulation challenges. 3.Proficient in literature mining (English journals/patents) with strong capability to extract, synthesize, and implement technical insights. 4.Intellectual curiosity and self-driven learning agility; embraces innovative/high-challenge tasks. 5.Hands-on experience with:Formulation equipment (e.g., fluid bed dryers, hot-melt extruders)DoE-based formulation screeningTechnical report writing. 6.Strong ethics, resilience in fast-paced environments, and collaborative mindset with excellent cross-functional communication skills.