Senior Research Associate – Biopharmaceutics (Pre-Formulation & Formulation Development)
Location: Bangalore, Karnataka, India
Company: Syngene International Ltd.
Division: Dedicated Centre
Department: Biopharmaceutics (BPH)
Employment Type: Full-Time
About the Company
Syngene International Ltd. is a globally recognized contract research, development, and manufacturing organization (CRDMO) delivering integrated scientific solutions across pharmaceuticals, biotechnology, nutrition, animal health, consumer goods, and specialty chemicals. With advanced research infrastructure and strategic partnerships with leading global pharmaceutical companies, Syngene supports accelerated drug discovery and development programs worldwide.
Job Overview
Syngene is seeking a Senior Research Associate (9-II) for its Biopharmaceutics team at BBRC, Bangalore. The role focuses on conducting pre-formulation studies and supporting phase-appropriate formulation development activities for preclinical and clinical programs.
This opportunity is ideal for professionals with strong expertise in physicochemical characterization, analytical techniques, and oral dosage formulation development within pharmaceutical R&D environments.
Experience Required
2–5 years of relevant industry experience in pre-formulation, formulation development, or pharmaceutical research
Experience handling new chemical entities (NCEs) in preclinical or early clinical stages preferred
Exposure to stability studies, solid-state characterization, and analytical instrumentation required
Educational Qualification
M.Pharm or M.S. in Pharmaceutics / Pharmaceutical Chemistry – Mandatory
Key Responsibilities
Pre-Formulation & Physicochemical Assessment
Conduct physicochemical property evaluation of new chemical entities (NCEs)
Perform pre-formulation studies to assess solubility, stability, compatibility, and solid-state properties
Utilize analytical instruments to characterize drug substances
Formulation Development Support
Develop and optimize formulations to support preclinical PK, PD, and toxicology studies
Assist in oral dosage form development including solutions, suspensions, tablets, and capsules
Conduct formulation feasibility and stability studies aligned with development phases
Data Analysis & Reporting
Record, summarize, and interpret experimental data
Prepare scientific and technical reports to support internal documentation and regulatory requirements
Ensure data integrity and compliance with quality standards
Cross-Functional Collaboration
Work closely with PK/PD, toxicology, medicinal chemistry, and analytical R&D teams
Support collaborative project execution within cross-functional research environments
Interact with client teams when required for project-specific discussions
Technical Skills
Strong understanding of physicochemical properties of drug substances
Knowledge of pre-formulation strategies and formulation development
Experience in analytical chemistry and solid-state characterization techniques
Familiarity with formulation stability studies and data interpretation
Proficiency in MS Office and scientific software tools used in pharmaceutical R&D
Behavioral & Functional Competencies
Strong written and verbal communication skills
Effective scientific presentation abilities
Team-oriented mindset with strong cross-functional collaboration
Analytical thinking and problem-solving capabilities
Why This Role?
This position offers hands-on exposure to early-phase drug development and formulation research in a globally recognized CRDMO environment. The role contributes directly to accelerating pharmaceutical R&D timelines while maintaining high scientific and quality standards.
Equal Opportunity Employer
Syngene International Ltd. is an equal opportunity employer committed to workplace diversity and inclusion. Employment decisions are based on merit and business requirements without discrimination based on legally protected characteristics. Reasonable accommodations are provided to qualified individuals with disabilities.
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