Method Development & Method Validation Expert
Brief Summary:
The role offers exposure to advanced analytical instrumentation, bioequivalence studies, regulated laboratory environments, and cutting-edge bioanalytical research projects.
Job Description:
🚀 WE’RE HIRING | Method Development & Method Validation Experts | Cliantha Research | Ahmedabad 🚀
Looking for exciting Bioanalytical Research jobs in Ahmedabad? Cliantha Research is hiring experienced professionals for its Bioanalytical Laboratory team.
This is an excellent opportunity for candidates with expertise in Method Development, Method Validation, LC-MS/MS, ICP-MS, and Bioanalysis who are looking to advance their careers in regulated bioanalytical research and bioequivalence studies.
🏢 Company: Cliantha Research
🌐 Industry: Clinical Research / Bioanalytical Research
👉 Role: Method Development & Method Validation Expert
💼 Experience: 2–7 Years
📍 Location: Ahmedabad, Gujarat
🏢 Work Mode: Work From Office
🕒 Employment Type: Full-Time
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🎓 Required Qualifications
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✔ M.Sc
✔ B.Pharm
✔ M.Pharm
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🎯 What We’re Looking For
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✔ Strong understanding of bioanalytical laboratory operations
✔ Hands-on experience with advanced analytical instrumentation
✔ Good analytical and problem-solving skills
✔ Knowledge of regulatory requirements and compliance standards
✔ Attention to detail and data accuracy
✔ Ability to work effectively in a team environment
✔ Strong documentation and communication skills
✔ Commitment to quality and scientific excellence
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🌟 Why Join Cliantha Research?
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✨ Opportunity to work on advanced bioanalytical research projects
✨ Exposure to cutting-edge analytical technologies
✨ Experience in regulated bioanalysis and bioequivalence studies
✨ Collaborative and research-focused work environment
✨ Career growth and continuous learning opportunities
✨ Opportunity to work with experienced scientific teams
✨ Exposure to global clinical research standards
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📩 Apply Now
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📧 srchauhan1@cliantha.com
🔁 Referrals are highly appreciated!
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⚡ If you have experience in Bioanalysis, Method Development, Method Validation, LC-MS/MS, and ICP-MS, Cliantha Research offers an excellent opportunity to grow your career in a highly regulated and research-driven environment.
Required Skills:
Key Responsibilities:
✔ Develop and validate bioanalytical methods in plasma, serum, and urine matrices
✔ Operate and troubleshoot LC-MS/MS instruments
✔ Operate and troubleshoot ICP-MS systems
✔ Conduct sample extraction using wet chemistry techniques
✔ Analyze subject samples from bioequivalence studies using validated methods
✔ Conduct literature searches to support method development activities
✔ Ensure compliance with regulated bioanalysis practices and regulatory guidelines
✔ Maintain laboratory documentation and analytical records
✔ Support quality, compliance, and audit readiness activities
About Cliantha Research
The organization is known for delivering high-quality scientific solutions through innovation, compliance, and operational excellence.
🚀 Core Focus Areas:
✅ Bioanalytical Research
✅ Clinical Research Services
✅ Bioequivalence Studies
✅ Method Development & Validation
✅ Central Laboratory Services
✅ Pharmacokinetic Analysis
✅ Regulatory-Compliant Research
✅ Drug Development Support
How to Apply / Contact Info
To apply for this position or make inquiries, please reach out directly to the employer at the contact email address below: