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Formulation Scientist

Syngene
Syngene
6-9 years
Not Disclosed
10 Dec. 29, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Formulation Scientist – Biopharmaceutical Development
Location: Bangalore, Karnataka, India
Experience Level: 6–9 years
Division: Development Services
Company: Syngene International Limited

About Syngene:
Syngene International Limited (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022) is a global contract research, development, and manufacturing organization (CRDMO) providing integrated solutions to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. With over 4,500 scientists and 1.9 million sq. ft. of state-of-the-art facilities, Syngene supports leading global companies including Amgen, Baxter, Bristol-Myers Squibb, GSK, Merck KGaA, and Herbalife in accelerating scientific discovery, formulation development, and quality manufacturing while ensuring data integrity and IP protection.

Position Overview:
Syngene is seeking an experienced Formulation Scientist to join its Development Services division in Bangalore. The ideal candidate will contribute to biologics parenteral formulation development, including early and late-stage development of monoclonal antibodies (mAbs), fusion proteins, and peptides. This role combines hands-on laboratory work, pre-formulation studies, stability analysis, and cross-functional collaboration, with the goal of delivering robust, regulatory-compliant formulations that meet global quality standards.

Key Responsibilities:

  • Design, develop, and optimize parenteral formulations for complex biologics.

  • Conduct pre-formulation studies using rational design principles, including buffer, excipient, and stabilizer screening.

  • Plan, execute, and analyze drug substance and drug product stability studies; interpret degradation kinetics and assign shelf-life.

  • Perform formulation and process characterization studies, including analysis of solid and liquid dosage forms.

  • Operate and maintain laboratory instrumentation such as Density Meters, Osmometers, Viscometers, Turbidity Meters, UV Spectrophotometers, and HPLC systems.

  • Author technical protocols, study reports, and product development reports, and effectively communicate outcomes to cross-functional teams.

  • Apply basic statistical analysis, Design of Experiments (DoE), and data visualization techniques to formulation studies.

  • Collaborate with internal teams for tech transfers, regulatory submissions, and process optimization.

  • Demonstrate strong problem-solving skills, scientific reasoning, and adherence to quality, safety, and compliance standards.

Required Qualifications & Experience:

  • M.Pharm or M.Sc. in Life Sciences, Biotechnology, Bioprocess Engineering, Pharmaceuticals, Biopharmaceuticals, Biopharmaceutical Technology, Biochemistry, or a related field.

  • 6–9 years of practical experience in formulation development for biopharmaceuticals, specifically with mAbs, fusion proteins, and peptides.

  • Hands-on expertise in parenteral formulation development, stability studies, and process characterization.

  • Proficiency in analytical instrumentation, formulation optimization, and regulatory-compliant documentation.

  • Strong analytical, organizational, and collaborative skills with the ability to deliver results under tight timelines.

Core Competencies & Skills:

  • Scientific rigor and methodical approach to formulation and stability studies.

  • Ability to troubleshoot complex formulation challenges and implement effective solutions.

  • Collaborative mindset with excellent communication skills to work in cross-functional and global teams.

  • Commitment to quality, safety, and continuous improvement in a regulated laboratory environment.

Why Join Syngene:

  • Opportunity to work with cutting-edge biologics and protein therapeutics in a GLP-compliant environment.

  • Exposure to early and late-stage formulation development with leading global biopharmaceutical clients.

  • Collaborative and innovative work culture promoting scientific growth and technical excellence.

Equal Opportunity Employer:
Syngene provides equal employment opportunities and reasonable accommodations to individuals with disabilities, fostering a diverse and inclusive workplace.

Learn More: Visit Syngene International to explore our services, capabilities, and career opportunities.

Apply Now to join Syngene as a Formulation Scientist and contribute to innovative biologics development.