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Drug Product Formulation Development Scientist

5+ years
₹10,00,000 – ₹20,00,000 per annum
10 Nov. 11, 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

Drug Product Formulation Development Scientist

Company: Lambda Therapeutic Research Ltd.
Req ID: 1293
Location: Ahmedabad, India
Date Posted: 5 Nov 2025
CTC Range: ₹10,00,000 – ₹20,00,000 per annum


Company Overview

Lambda Therapeutic Research Limited is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India, with operations in:

  • Mehsana (India)

  • Warsaw (Poland)

  • London (UK)

  • Pittsburgh (USA)

  • Las Vegas (USA)

  • Fargo (USA)

The company provides end-to-end clinical trial solutions with over 20 years of experience in the biopharmaceutical and generic industries. Lambda emphasizes quality, innovation, and technical expertise to help clients develop products safely and effectively.


Job Summary

The Drug Product Formulation Development Scientist is responsible for designing and executing formulation development studies for drug products (DP) within the Process Sciences group, focusing on liquid and lyophilized (lyo) dosage forms with desired physicochemical characteristics.


Key Responsibilities

  • Provide technical leadership for DP formulation and lyophilization development and characterization.

  • Design formulation studies and select appropriate excipients for different dosage forms (liquid/lyo) and stability studies.

  • Perform primary packaging container selection and execute compatibility studies.

  • Conduct forced product degradation studies.

  • Apply knowledge of DP unit operations: freeze/thaw, filtration, mixing, filling, lyophilization, container closure integrity testing, and packaging.

  • Collaborate effectively with clients and internal cross-functional teams.

  • Author and review technical reports related to drug products.

  • Contribute to regulatory submissions, audits, and publications/IP concerning formulations.


Experience Required

  • Minimum 5+ years in drug product formulation development and manufacturing.

  • Strong understanding of formulation study design, excipient selection, and stability studies.

  • Knowledge of DP unit operations and packaging is highly desirable.

  • Cross-functional technical knowledge preferred.

  • Excellent oral and written communication and interpersonal skills.


Educational Qualification

  • Master’s or Ph.D. in Chemical/Biochemical Engineering or similar disciplines.