Job Overview
| Particulars | Details |
|---|---|
| Position | Research Executive |
| Company | |
| Job Type | |
| Category / Department | Research |
| Application Mode |
🏢 About
📍 Location: Ahmedabad, Gujarat, India
💡 Editor's Note / Preparation Tip
📄 Resume Preparation Tips
1️⃣ Clearly highlight your 2+ years of Method Validation report writing experience.
2️⃣ Mention specific experience with PK, PD, immunogenicity, small molecules, biologics, or biosimilars.
3️⃣ Showcase your knowledge of GLP, non-GLP guidelines, regulatory documentation, and scientific report writing.
4️⃣ Include experience working with QC and QA teams and resolving review queries.
5️⃣ Highlight your experience in SOP preparation, report tracking, data compilation, and cross-functional coordination.
🎯 Interview Preparation
1️⃣ Revise the fundamentals of method validation and understand key validation parameters.
2️⃣ Prepare to explain your experience writing MV reports for PK, PD, immunogenicity, small molecules, biologics, or biosimilars.
3️⃣ Review the differences between GLP and non-GLP environments and their documentation requirements.
4️⃣ Be ready to explain how you handle QC/QA comments, review queries, discrepancies, and report revisions.
5️⃣ Prepare real examples demonstrating your ability to manage multiple reports and meet strict documentation timelines.
💡 Professional Tips
1️⃣ Strengthen your knowledge of bioanalytical method validation principles and regulatory expectations.
2️⃣ Understand how method validation data is generated, compiled, reviewed, and presented in final reports.
3️⃣ Develop strong scientific writing skills focused on clarity, accuracy, consistency, and traceability.
4️⃣ Learn how to efficiently manage document versions, review cycles, and approval workflows.
5️⃣ During interviews, demonstrate your ability to balance scientific accuracy, regulatory compliance, quality, and deadlines.
📝 Job Description
Here’s the polished LinkedIn hiring post in the same format, with the section separators removed from all labels:
🚀 Research Executive | Lambda Therapeutic Research Ltd.
🧪 Exciting Opportunity for Life Science Professionals in Ahmedabad!
Lambda Therapeutic Research Ltd., a global full-service Clinical Research Organization, is hiring a Research Executive in Ahmedabad. This opportunity is ideal for professionals with 2+ years of experience in Method Validation (MV) report writing, particularly across PK, PD, immunogenicity assays, small molecules, biologics, and biosimilars.
If you have a strong background in scientific documentation and are experienced in preparing regulatory-compliant method validation reports under GLP and non-GLP guidelines, this could be an excellent opportunity to grow your career in clinical research, bioanalytical reporting, and scientific documentation. 🔬📄
Position Details
Company: Lambda Therapeutic Research Ltd.
Position: Research Executive
Requisition ID: 1584
Location: Ahmedabad, India
Job Type: Full-Time
Experience: 2+ Years
Qualification: MSc in Biotechnology, Biochemistry, or Life Science
Salary: ₹4,00,000 – ₹8,00,000 per year
Posted Date: July 26, 2026
Last Date: Not Specified
Work Mode: Not Specified
Role Focus: Method Validation Report Writing
Short Description
Lambda Therapeutic Research Ltd. is looking for a Research Executive with strong experience in Method Validation report writing. The selected candidate will prepare MV reports for PK, PD, and immunogenicity assays, covering areas such as small molecules, biologics, and biosimilars. The role requires a solid understanding of GLP and non-GLP regulatory guidelines and strong scientific documentation skills. The candidate will collaborate with Operations, Quality Control, and Quality Assurance teams to compile data, address review queries, and finalize reports. This is a strong opportunity for life science professionals seeking to advance their careers in clinical research documentation, bioanalytical reporting, and regulatory-compliant scientific writing.
Required Skills
✔️ Method Validation (MV) Report Writing
✔️ PK / PD Assay Documentation
✔️ Immunogenicity Assay Reporting
✔️ GLP and Non-GLP Guideline Knowledge
✔️ Scientific Report Writing and Formatting
✔️ Regulatory-Compliant Documentation
✔️ SOP Preparation and Maintenance
✔️ QC and QA Review Coordination
✔️ Method Validation Data Compilation
✔️ Documentation Accuracy and Quality Control
✔️ Timeline and Report Tracking
Preferred Skills
⭐ Experience with small molecule studies
⭐ Experience with biologics and biosimilar studies
⭐ Knowledge of bioanalytical method validation
⭐ Experience in clinical research documentation
⭐ Familiarity with QC and QA review processes
⭐ Understanding of regulatory requirements for scientific reports
⭐ Experience handling review comments and resolving queries
⭐ Knowledge of SOP development and maintenance
Detailed Job Description / Responsibilities
• Prepare Method Validation reports for PK, PD, and immunogenicity assays.
• Write MV reports for small molecules, biologics, and biosimilars in accordance with applicable GLP and non-GLP regulatory guidelines.
• Coordinate with Operations teams to collect and compile relevant method validation data.
• Work closely with Quality Control and Quality Assurance teams to facilitate QC and QA review of MV reports.
• Review and resolve QC and QA queries related to method validation report preparation.
• Ensure proper formatting, completeness, review readiness, and finalization of MV reports.
• Track and monitor method validation report timelines to ensure timely completion.
• Prepare, update, and maintain SOPs related to Method Validation report writing.
• Maintain accurate documentation and records throughout the report preparation and review lifecycle.
• Coordinate with cross-functional teams to ensure high-quality and regulatory-compliant deliverables.
Candidate Requirements
🎓 MSc in Biotechnology
🎓 MSc in Biochemistry
🎓 MSc in Life Science
💼 Minimum 2+ years of relevant experience
🧪 Experience in Method Validation report writing is required.
🔬 Experience with small molecules, biologics, or biosimilars is highly relevant.
📄 Knowledge of preparing scientific reports according to GLP and non-GLP regulatory guidelines.
🤝 Ability to coordinate effectively with Operations, QC, and QA teams.
⏱️ Strong timeline management and attention to detail.
✍️ Excellent scientific writing and documentation skills.
Why Join Lambda Therapeutic Research Ltd.?
🌍 Work with a global full-service Clinical Research Organization
🔬 Build specialized expertise in bioanalytical and method validation documentation
🧪 Gain exposure to PK, PD, immunogenicity, small molecules, biologics, and biosimilars
📚 Strengthen your understanding of GLP and non-GLP regulatory documentation
🤝 Collaborate with Operations, QC, and QA professionals
📈 Develop expertise in scientific and regulatory-compliant report writing
💼 Build a career in clinical research and bioanalytical documentation
🚀 Work in a specialized role with opportunities to expand your life sciences expertise
About Lambda Therapeutic Research Ltd.
Company Overview
Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) supporting pharmaceutical, biotechnology, and healthcare research programs. The organization operates in the clinical research and bioanalytical space, providing specialized capabilities that support the development of pharmaceutical and healthcare products.
Company Mission
The organization focuses on supporting the development of innovative healthcare solutions through scientific expertise, quality-driven research processes, and reliable clinical and bioanalytical services.
Company Vision
Lambda Therapeutic Research aims to contribute to the global healthcare ecosystem by providing high-quality research services that help advance pharmaceutical and biotechnology development.
Core Values
🔹 Scientific excellence
🔹 Quality and compliance
🔹 Integrity and accountability
🔹 Patient and public health focus
🔹 Innovation and continuous improvement
🔹 Collaboration and teamwork
🔹 Commitment to regulatory standards
What Makes Them Different
Lambda Therapeutic Research operates across the clinical research and bioanalytical landscape, providing professionals with exposure to specialized scientific areas. This role offers the opportunity to work on method validation reports involving PK, PD, immunogenicity, small molecules, biologics, and biosimilars, making it particularly relevant for professionals interested in scientific and regulatory documentation.
Leadership / Company Philosophy
The organization’s work emphasizes scientific rigor, quality, regulatory compliance, and collaboration across specialized teams. Employees work alongside Operations, Quality Control, Quality Assurance, and scientific professionals to deliver accurate and compliant research documentation.
Company Address
Frequently Asked Questions (FAQ)
Editor Notes | Resume Tips | Interview Preparation | Pro Tips
How to Apply
📩 Interested candidates can apply through the official Lambda Therapeutic Research Ltd. career portal.
🔎 Requisition ID: 1584
📍 Location: Ahmedabad, India
💼 Position: Research Executive
🧪 Experience: 2+ Years
Know someone who would be a great fit? Tag them or share this opportunity with your network! 🚀
🚀 Career Guidance & Interview Insights
To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.
This Research Executive role offers a dynamic work environment designed for professional growth. You will collaborate with experienced professionals, contribute to critical projects, and build transferable skills in communication, project management, and strategic execution. It is an excellent step for anyone seeking to advance their career.
Standard career growth starts in Junior/Associate executive roles, mastering foundational deliverables. After 3-5 years, professionals move to Senior Coordinator or Team Lead, supervising projects. Long-term progress leads to General Manager, Business Unit Director, and executive management roles focused on strategic organizational growth.
Expected Technical & Behavioral Questions:
- Q1: How do you handle working under tight deadlines with competing priorities?
Answer Tip: Discuss task prioritization, breaking down assignments, eliminating distractions, and proactively communicating roadblocks to the manager. - Q2: Describe a time you resolved a conflict with a co-worker.
Answer Tip: Emphasize active listening, finding common ground, keeping communication professional, and focusing on business outcomes. - Q3: What methods do you use to track your daily progress and productivity?
Answer Tip: Mention checklists, time-blocking, task management apps (like Trello/Asana), and reviewing daily outcomes against weekly goals.
To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:
- Keywords to include: Project Management, Stakeholder Communication, Time Management, Problem Solving, MS Office Suite, Documentation, Collaboration.
- Format: Keep the resume to 1-2 pages maximum. Use standard fonts like Inter, Arial, or Calibri (10-12pt text).
- Quantify Results: E.g., 'Managed 3 cross-functional team projects, delivering all milestones 2 weeks ahead of schedule.'
Estimated compensation for this role type in India is ₹2,20,000 - ₹3,60,000 per annum. The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.
To boost your professional profile, look into: Project Management Professional (PMP), CAPM from PMI, Certified ScrumMaster (CSM), or advanced business communications and spreadsheet management credentials.
Frequently Asked Questions
1️⃣ Where is the Research Executive position located?
The position is based in Ahmedabad, India.
2️⃣ How much experience is required?
Candidates should have 2+ years of relevant experience, particularly in Method Validation report writing.
3️⃣ What educational qualification is required?
Candidates should have an MSc in Biotechnology, Biochemistry, or Life Science.
4️⃣ What type of report writing experience is preferred?
Experience preparing Method Validation reports for PK, PD, immunogenicity assays, small molecules, biologics, or biosimilars is highly relevant.
5️⃣ What salary is offered for this role?
The listed salary range is ₹4,00,000 – ₹8,00,000 per year, depending on experience, report writing expertise, and relevant exposure.
6️⃣ What are the key regulatory requirements involved in the role?
The role requires knowledge of preparing Method Validation reports according to applicable GLP and non-GLP regulatory guidelines.
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