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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 Formulation | Bengaluru, India

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


About Syngene

Syngene International Ltd. (BSE: 539268, NSE: SYNGENE) is a globally integrated research, development, and manufacturing solutions organization serving the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. With over 4,500 scientists and 1.9 million sq. ft. of specialist facilities, Syngene partners with global leaders including Amgen, Baxter, Bristol-Myers Squibb, Herbalife, GSK, and Merck KGaA, delivering high-quality science, robust data management, IP security, and accelerated time-to-market.

Syngene offers a collaborative, innovation-driven culture and the opportunity to work on complex biologics, mAbs, fusion proteins, and biopharmaceutical formulations.


Role Overview

The Formulation Scientist will be responsible for designing, developing, and optimizing parenteral formulations for biologics. This role includes pre-formulation studies, stability assessment, formulation characterization, and technical documentation, supporting both early and late-stage development of monoclonal antibodies (mAbs), proteins, and peptides. The position demands hands-on laboratory experience, analytical expertise, and strong cross-functional collaboration skills.


Key Responsibilities

Formulation & Pre-Formulation:

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

  • Conduct pre-formulation studies, including buffer, excipient, and stabilizer screening, structure-function assessment, and rational formulation design.

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

Analytical & Process Characterization:

  • Handle analytical instruments such as Density meter, Osmometer, Viscometer, Turbidity meter, UV Spectrophotometer, and HPLC systems.

  • Perform formulation and process characterization studies, supporting robust product development.

  • Apply basic statistical analysis, Design of Experiments (DoE), and data visualization to evaluate experimental outcomes.

Documentation & Communication:

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

  • Communicate study outcomes effectively with cross-functional teams, ensuring clarity and adherence to timelines.

Collaboration & Compliance:

  • Work collaboratively with cross-functional teams to ensure formulation strategies align with regulatory standards and project goals.

  • Demonstrate commitment to quality, safety, and EHS standards in laboratory operations.


Required Qualifications & Experience

  • Education: M.Pharm or M.Sc. in Life Science, 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.


Behavioral Competencies

  • Positive, proactive, and enthusiastic approach to problem-solving.

  • Strong scientific reasoning and logical thinking.

  • Ability to work independently and collaboratively in a team environment.

  • Flexible and able to deliver quality results under tight timelines.

  • Effective communication and interpersonal skills.


Equal Opportunity Employer

Syngene is committed to equal employment opportunity (EEO) for all applicants, 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 available 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.