Analytical Development Laboratory Executive

Drlogy; Ahmedabad District; On-site; INR 400,000 - 600,000; Full time

Job summary

Drlogy is looking for an Analytical Development Laboratory Executive in Ahmedabad, India. The role involves developing and optimizing analytical methods for pharmaceuticals, ensuring compliance with regulations, and working with cross-functional teams to support product development.

The ideal candidate should possess a strong background in analytical chemistry with experience in methods such as HPLC and GC. The position is crucial for maintaining data integrity and laboratory safety.

Qualifications

• Strong knowledge of analytical chemistry and related techniques.
• Experience in analytical testing and method validation.
• Ability to interpret analytical data and trends accurately.

Responsibilities

• Develop and optimize analytical methods for pharmaceutical products.
• Conduct method validation and robustness studies.
• Ensure compliance with GLP, GMP, and laboratory safety standards.

Skills

Analytical method development

HPLC

GC

UV

Dissolution

Impurity profiling

Regulatory documentation

Tools

FTIR

Job description

Analytical Development Laboratory Executive

The Analytical Development Laboratory Executive will be responsible for analytical method development, method validation, sample analysis, documentation, and technical support for pharmaceutical development projects. This requires strong knowledge of analytical chemistry, HPLC, GC, UV, dissolution, impurity profiling, and regulatory documentation. The candidate will work closely with formulation, QA, QC, and R&D teams to generate reliable analytical data and support product development and regulatory requirements.

Responsibilities

• Develop and optimize analytical methods for pharmaceutical products, intermediates, and raw materials.
• Perform analytical testing using instruments such as HPLC, GC, UV, FTIR, and dissolution apparatus.
• Conduct method validation, verification, transfer, and robustness studies as per guidelines.
• Analyze samples for assay, impurities, dissolution, content uniformity, and stability studies.
• Prepare standards, reagents, mobile phases, buffers, and sample solutions accurately.
• Interpret chromatograms, analytical data, trends, and test results with scientific accuracy.
• Maintain raw data, worksheets, instrument logs, analytical reports, and method development records.
• Troubleshoot analytical methods, instrument issues, peak abnormalities, and result variations.
• Coordinate with formulation, QC, QA, and regulatory teams for project requirements.
• Support stability studies, forced degradation studies, and impurity profiling activities.
• Ensure compliance with GLP, GMP, data integrity, and laboratory safety requirements.
• Review analytical specifications, test methods, protocols, and validation documents.
• Participate in investigations related to OOS, OOT, deviations, and analytical failures.
• Maintain laboratory instruments, columns, standards, and consumables in ready condition.
• Prepare accurate analytical summaries and technical reports for internal and regulatory use.