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Deputy Manager

Lambda Research Accelerated
Lambda Research accelerated
6-10 years
INR 10,00,000 – 15,00,000 per annum
Ahmedabad, India
10 March 6, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Job Title: Deputy Manager

Company: Lambda Therapeutic Research Ltd.

Location: Ahmedabad, India

Job ID: 1501

Employment Type: Full-Time

CTC Range: INR 10,00,000 – 15,00,000 per annum

Experience Required: 6–10 years

About the Company
Lambda Therapeutic Research Limited is a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad, India. The organization operates advanced research facilities in Mehsana (India), Warsaw (Poland), London (UK), Pittsburgh (USA), Las Vegas (USA), and Fargo (USA), employing more than 1,500 professionals worldwide.

With over two decades of industry experience, Lambda provides full-spectrum clinical trial and drug development services to global biopharmaceutical, biotechnology, and generic pharmaceutical companies. The organization leverages scientific expertise, innovative technologies, and strong regulatory compliance to accelerate the development of safe, effective, and high-quality therapeutic products.

Job Overview
Lambda Therapeutic Research Ltd. is seeking an experienced Deputy Manager to join the Process Sciences team. The selected candidate will play a key role in designing, executing, and analyzing experiments related to monoclonal antibody (mAb) downstream processing. The role involves leading purification development activities and managing multiple unit operations involved in the production of clinical-grade drug substances.

The ideal candidate will contribute technical expertise to support process development, optimization, and technology transfer activities while ensuring compliance with regulatory and quality standards.

Key Responsibilities

  • Design, plan, and execute experiments related to monoclonal antibody downstream processing and purification development.

  • Lead and manage a team responsible for purification unit operations for clinical-grade drug substance manufacturing.

  • Evaluate emerging technologies to develop cost-effective capture and purification strategies for monoclonal antibodies.

  • Oversee operation and maintenance of purification skids and chromatography columns across laboratory, pilot, and manufacturing scales.

  • Utilize automation software tools for purification processes and ensure efficient system operation.

  • Apply statistical analysis and process evaluation tools to monitor process performance and consistency.

  • Collaborate with Contract Research Organizations (CROs) to coordinate viral clearance studies.

  • Author and review technical documentation related to purification processes, viral clearance studies, and regulatory submissions supporting IND-enabling activities.

  • Establish and maintain a comprehensive library of purification materials including chromatography resins and filtration systems.

  • Support technology transfer of developed purification processes to pilot-scale or GMP manufacturing facilities.

  • Ensure downstream process development activities comply with GMP standards and regulatory requirements.

Technical Skills

  • Strong expertise in monoclonal antibody purification and downstream process development.

  • Knowledge of chromatography-based purification techniques and filtration technologies.

  • Familiarity with purification automation software and data analysis tools.

  • Experience in viral clearance study coordination and regulatory documentation.

  • Understanding of GMP-compliant manufacturing and process transfer activities.

Soft Skills

  • Strong leadership and team management capabilities.

  • Excellent analytical and problem-solving skills.

  • Effective communication and technical reporting abilities.

  • Strong collaboration skills for cross-functional and external partnerships.

Educational Qualification
Bachelor’s degree in Biochemical Engineering or Chemical Engineering with M.Tech or PhD in Biochemical Engineering, Biological Sciences, or a related discipline.

Job Category: Biopharmaceutical Process Development / Downstream Processing / Clinical Research

How to Apply
Qualified candidates interested in advanced roles in biopharmaceutical process development are encouraged to apply through the official careers portal of Lambda Therapeutic Research Ltd. or explore similar global pharmaceutical opportunities on ThePharmaDaily.com.