Formulation Scientist
Location: Bangalore, Karnataka, India
Division: Development Services
Employment Type: Full-Time
Company Overview:
Syngene International Ltd. (BSE: 539268, NSE: SYNGENE) is a leading integrated research, development, and manufacturing solutions company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. With over 4,500 scientists and 1.9 million sq. ft. of dedicated discovery, development, and manufacturing facilities, Syngene delivers high-quality science, robust data management, and IP-secure solutions to accelerate innovation and improve time-to-market for its global clients, including Amgen, Baxter, GSK, Bristol-Myers Squibb, Merck KGaA, and Herbalife.
Role Summary:
We are seeking an experienced Formulation Scientist to join our Development Services team in Bangalore. The ideal candidate will specialize in parenteral formulation development of biologics, including monoclonal antibodies (mAbs), fusion proteins, and peptides, and will contribute across early and late-stage formulation projects.
Key Responsibilities:
Design and develop parenteral formulations for complex biologics, both solid and liquid dosage forms.
Execute pre-formulation studies using rational design principles, including structure-function assessment, buffer/excipient/stabilizer screening, and stability evaluations.
Plan and conduct drug substance/product stability studies, analyze data trends, and support shelf-life assignment.
Author protocols, technical reports, and communicate study outcomes to cross-functional teams.
Perform formulation and process characterization studies, including analytical and biophysical assessments.
Operate and manage laboratory instruments such as density meters, osmometers, viscometers, turbidity meters, UV spectrophotometers, and HPLC systems.
Apply basic statistical analysis, Design of Experiments (DoE), and data visualization in study evaluations.
Support technical documentation, including Product Development Reports (PDRs), technology transfer documents, and study reports.
Experience & Requirements:
Minimum 6–9 years of practical experience in biopharmaceutical formulation development.
Strong expertise in parenteral formulation of biologics, including mAbs, fusion proteins, and peptides.
Hands-on experience in both early and late-stage formulation development.
Proficiency in formulation and process characterization studies.
Demonstrated ability to author technical documents and communicate effectively with cross-functional teams.
Educational Qualification: M.Pharm or M.Sc. in Life Sciences, Biotechnology, Bioprocess Engineering, Biopharmaceuticals, Pharmaceuticals, Biochemistry, or equivalent degree.
Positive attitude, logical thinking, strong work ethic, and commitment to delivering high-quality results.
Why Syngene:
Syngene provides an inclusive, innovative, and collaborative work environment where scientists are empowered to grow professionally while delivering cutting-edge solutions for global pharmaceutical clients. Join us to contribute to transformative biopharmaceutical development and make a meaningful impact on patient care worldwide.
Equal Opportunity Employer:
Syngene International is an Equal Employment Opportunity (EEO) employer. We are committed to providing reasonable accommodations to qualified individuals with disabilities and fostering an inclusive workplace free from discrimination based on age, color, national origin, citizenship, disability, race, religion, gender, sexual orientation, gender identity, genetic information, marital status, veteran status, or any other legally protected status.
Learn More: Syngene International
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