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Formulation Scientist

Syngene
Syngene
6-9 years
Not Disclosed
10 Jan. 6, 2026
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 – Biologics Parenteral Development | Bengaluru, India

Company: Syngene International Limited
Location: Bengaluru, Karnataka, India
Division: Development Services
Experience Required: 6–9 years
Job Type: Full-Time


About Syngene

Syngene International Ltd. (BSE: 539268, NSE: SYNGENE) is a leading integrated research, development, and manufacturing solutions organization serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors.

With a team of 4,500+ scientists and 1.9 million sq. ft. of specialized discovery, development, and manufacturing facilities, Syngene partners with global industry leaders including Amgen, Baxter, Bristol-Myers Squibb, Herbalife, GSK, and Merck KGaA, delivering innovative science, robust data management, IP security, and accelerated time-to-market.


Role Overview

We are seeking an experienced Formulation Scientist to join our Development Services team in Bengaluru. This role focuses on designing and developing parenteral formulations for complex biologics, including monoclonal antibodies (mAbs), proteins, and fusion proteins. The position offers an opportunity to lead pre-formulation studies, stability assessments, process characterization, and technical documentation, ensuring high-quality, compliant biopharmaceutical development.


Key Responsibilities

Formulation Development:

  • Design and develop parenteral formulations for biologics, including solid and liquid dosage forms.

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

  • Plan and execute drug substance/product stability studies, analyze data trends, and support shelf-life assignment.

Analytical & Process Characterization:

  • Perform formulation and process characterization studies.

  • Operate analytical instruments including Density meter, Osmometer, Viscometer, Turbidity meter, UV Spectrophotometer, and HPLC systems.

  • Apply basic statistical methods, Design of Experiments (DoE), and data visualization for experimental analysis.

Documentation & Reporting:

  • Author protocols, technical reports, study reports, PDRs, and tech transfer documents.

  • Communicate study outcomes to cross-functional teams effectively.

Collaboration & Compliance:

  • Work closely with cross-functional teams, ensuring adherence to regulatory standards, internal SOPs, and quality requirements.

  • Demonstrate positive, proactive, and results-oriented work ethic, maintaining project timelines and deliverables.


Required Qualifications & Experience

  • Education: M.Pharm or M.Sc. in Life Sciences, Biotechnology, Bioprocess Engineering, Pharmaceuticals, Biopharmaceuticals, Biopharmaceutical Technology, Biochemistry, or equivalent.

  • Experience: 6–9 years in biopharmaceutical formulation development, specifically with mAbs, proteins, and peptides.

  • Strong expertise in parenteral formulation, process characterization, and analytical techniques.

  • Proven experience in technical documentation and regulatory compliance.


Core Competencies

  • Strong scientific reasoning, logical thinking, and problem-solving skills.

  • Ability to work independently and collaboratively in a fast-paced environment.

  • Effective communication and interpersonal skills.

  • Positive, committed, and detail-oriented approach to deliver high-quality results.


Equal Opportunity Employer

Syngene is committed to equal employment opportunity (EEO) for all candidates, irrespective of age, color, national origin, citizenship, disability, race, religion, gender, sexual orientation, gender identity, veteran status, or any legally protected characteristic. Reasonable accommodations are provided for qualified individuals with disabilities.


Apply Now to join Syngene’s Development Services team in Bengaluru and contribute to cutting-edge biologics formulation and biopharmaceutical innovation.

Learn more about Syngene: https://syngeneintl.com