Job Title: Drug Product Formulation Development Scientist
Req ID: 1293
Date: January 2, 2026
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range (INR): 1,000,000 – 2,000,000
Lambda Therapeutic Research Ltd. is a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad, India, with facilities in Mehsana (India), Warsaw (Poland), London (UK), Pittsburgh (USA), Las Vegas (USA), and Fargo (USA). With over 1,500 employees worldwide, Lambda provides comprehensive clinical trial solutions to the biopharmaceutical and generic pharmaceutical industries.
With more than 20 years of expertise, we combine innovative technologies, therapeutic knowledge, and a strong commitment to quality to help clients develop products safely, efficiently, and successfully. Our people are the foundation of our excellence, and we are committed to hiring highly qualified and energetic individuals to join our team.
We are seeking a Drug Product Formulation Development Scientist to lead formulation development studies within the Process Sciences group. This role is critical in designing and delivering suitable formulations in liquid and lyophilized dosage forms with desired physicochemical characteristics, stability, and manufacturability.
Provide technical leadership for drug product (DP) formulation and lyophilization development and characterization.
Design and execute formulation studies, selecting appropriate excipients for different dosage forms (liquid/lyo) and performing stability studies to ensure product quality.
Conduct selection and compatibility studies for primary packaging containers.
Perform forced degradation studies to assess product stability and robustness.
Apply knowledge of DP unit operations including freeze-thaw, filtration, filling, lyophilization, mixing, and container closure integrity testing.
Collaborate effectively with internal teams and clients to support project objectives.
Author and review technical reports related to drug product formulation, contributing to regulatory submissions and audits.
Support intellectual property development and scientific publications related to drug product formulations.
Strong understanding of design of formulation studies, excipient selection, and stability studies for liquid and lyophilized dosage forms.
Practical knowledge of DP unit operations: freeze-thaw, filling, filtration, mixing, lyophilization, packaging, and container closure integrity testing.
Cross-functional technical knowledge in formulation development and drug manufacturing is highly desirable.
Excellent oral and written communication, interpersonal skills, and ability to work collaboratively with teams and clients.
Masters or Ph.D. in Chemical Engineering, Biochemical Engineering, or related discipline.
Minimum 5+ years of work experience in drug product formulation development and manufacturing.
Opportunity to work in a global CRO with exposure to cutting-edge drug formulation and process science.
Lead development of innovative formulations for global clients, contributing to regulatory submissions and scientific publications.
Career growth through mentorship, cross-functional collaboration, and hands-on experience in drug product development and manufacturing.
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