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., established in 1993, is a global innovation-led contract research, development, and manufacturing organization (CRDMO). The company delivers integrated scientific services across pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors.
With a strong global client base including leading multinational pharmaceutical organizations, Syngene supports discovery, development, and commercialization programs through advanced scientific infrastructure and a highly skilled research workforce.
Job Overview
Syngene is hiring a Senior Research Associate (9-II) for its Biopharmaceutics team at BBRC, Bangalore. The role focuses on pre-formulation studies and phase-appropriate formulation development to support preclinical and clinical research programs.
This position is ideal for professionals with a strong academic background in pharmaceutics or pharmaceutical chemistry who possess hands-on experience in physicochemical characterization and formulation development of new chemical entities (NCEs).
Experience Required
2–5 years of relevant experience in pre-formulation, formulation development, or pharmaceutical R&D
Experience working with NCEs in preclinical or early clinical development stages preferred
Exposure to analytical instrumentation and solid-state characterization techniques is desirable
Educational Qualification
M.Pharm or M.S. in Pharmaceutics / Pharmaceutical Chemistry – Mandatory
Key Responsibilities
Pre-Formulation & Physicochemical Characterization
Conduct physicochemical property assessment of new chemical entities (NCEs)
Perform pre-formulation studies to evaluate solubility, stability, and compatibility
Utilize analytical tools and instruments to characterize drug substances
Support solid-state characterization studies
Formulation Development
Develop and optimize formulations for preclinical pharmacokinetics (PK), pharmacodynamics (PD), and toxicology studies
Assist in oral drug product development for clinical studies, including solutions, suspensions, tablets, and capsules
Conduct formulation feasibility and stability studies
Data Documentation & Reporting
Record, analyze, and interpret experimental data
Prepare scientific and technical reports to support regulatory and internal documentation
Maintain accurate laboratory records in compliance with quality and data integrity standards
Cross-Functional Collaboration
Work closely with PK/PD, toxicology, medicinal chemistry, and analytical R&D teams
Engage with internal and external stakeholders, including client teams in discovery and development pharmaceutics
Contribute to collaborative project execution and milestone delivery
Technical Skills Required
Strong understanding of physicochemical properties of drug substances
Expertise in pre-formulation and formulation development
Knowledge of analytical chemistry and solid-state characterization techniques
Experience in formulation stability studies and data interpretation
Proficiency in MS Office and basic scientific software used in pharmaceutical R&D
Behavioral & Functional Competencies
Strong written and verbal communication skills
Scientific presentation and documentation capability
Team-oriented mindset with cross-functional collaboration skills
Proactive learner with strong problem-solving abilities
Why Join This Role?
This position offers exposure to early-phase drug development programs, including preclinical and clinical formulation support. It provides an opportunity to work in a highly collaborative pharmaceutical R&D environment contributing to accelerated drug development timelines and innovation-driven scientific solutions.
Equal Opportunity Employer
Syngene International Ltd. is an equal opportunity employer committed to diversity and inclusion. Employment decisions are based on merit and business needs, without discrimination based on legally protected characteristics. Reasonable accommodations are provided to qualified individuals with disabilities.
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