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2+ years
4 LPA - 8 LPA
Ahmedabad, India
1 June 30, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

Research Executive

Company: Lambda Therapeutic Research Ltd.
Location: Ahmedabad, India
Department: Bioanalytical Research / Method Validation
Job Type: Full-Time
CTC: ₹4 LPA – ₹8 LPA

JOB OVERVIEW

The Research Executive is responsible for preparing and managing Method Validation (MV) reports for small molecule, pharmacokinetic (PK), pharmacodynamic (PD), and immunogenicity assays in accordance with GLP and non-GLP regulatory guidelines. The role involves compiling bioanalytical data, coordinating with laboratory operations, Quality Control (QC), and Quality Assurance (QA) teams, ensuring accurate report formatting, maintaining documentation, managing timelines, and developing Standard Operating Procedures (SOPs) to support regulatory-compliant bioanalytical method validation activities.


KEY RESPONSIBILITIES

Method Validation Report Writing

  • Prepare Method Validation (MV) reports for PK, PD, and Immunogenicity assays.

  • Develop reports for small molecule and ligand binding assay (LBA) studies.

  • Ensure reports comply with GLP and non-GLP regulatory requirements.

  • Review validation data for completeness and accuracy.

  • Finalize validation reports for regulatory submission.

Bioanalytical Documentation

  • Compile bioanalytical data required for MV reports.

  • Maintain accurate and organized validation documentation.

  • Ensure proper report formatting and version control.

  • Archive completed validation reports.

  • Maintain documentation in accordance with company procedures.

Cross-Functional Coordination

  • Coordinate with laboratory operations teams to collect study data.

  • Collaborate with Quality Control (QC) for report review.

  • Work with Quality Assurance (QA) during report approval.

  • Resolve QC and QA review comments promptly.

  • Communicate project status with internal stakeholders.

Quality & Regulatory Compliance

  • Ensure compliance with GLP and applicable regulatory guidelines.

  • Support inspection-ready documentation.

  • Maintain quality standards throughout report preparation.

  • Follow company Standard Operating Procedures (SOPs).

  • Support continuous quality improvement initiatives.

Timeline & Project Management

  • Track method validation activities and report progress.

  • Monitor report preparation timelines.

  • Ensure timely completion of validation documentation.

  • Prioritize multiple report preparation activities.

  • Support project scheduling and workflow management.

SOP Management

  • Prepare and update Standard Operating Procedures (SOPs).

  • Maintain SOP documentation related to MV report preparation.

  • Ensure SOPs reflect current regulatory requirements.

  • Support implementation of revised procedures.

  • Participate in process improvement initiatives.


EDUCATIONAL QUALIFICATIONS

Required

Master's Degree in:

  • Biotechnology

  • Biochemistry

  • Life Sciences

  • Or a related discipline


EXPERIENCE REQUIREMENTS

Required

  • Minimum 2 years of experience in:

    • Method Validation Report Writing

    • Bioanalytical Research

    • PK/PD Assays

    • Immunogenicity Assays

Preferred

  • Experience with small molecule bioanalysis.

  • Experience with biologics and biosimilars.

  • Knowledge of Ligand Binding Assays (LBA).

  • Experience in CRO or pharmaceutical laboratories.

  • Familiarity with regulatory documentation and inspections.