Scientist – Bioresearch Laboratory (Small Molecule Bioanalytical Research)
Location: Bangalore, Karnataka, India
Company: Syngene International Ltd.
Division: Discovery Services
Department: Translational and Clinical Research – Small Molecule Bioanalytical Laboratory
Employment Type: Full-Time
Reporting To: Project Leader / Group Leader
About the Company
Syngene International Ltd. is a leading integrated research, development, and manufacturing solutions organization serving global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries. With advanced discovery and bioanalytical infrastructure and a strong team of scientific professionals, Syngene supports accelerated drug development, regulatory compliance, and high-quality data generation across clinical and preclinical programs.
Job Overview
Syngene is hiring a Scientist – Bioresearch Laboratory (Research Associate / Executive / Analyst level) for its Small Molecule Bioanalytical Research Laboratory in Bangalore. This role is responsible for conducting regulated bioanalytical studies, including BA/BE (Bioavailability/Bioequivalence) studies, method development, validation, and study sample analysis in compliance with GLP/GCP guidelines.
The position requires strong expertise in small molecule bioanalysis, analytical instrumentation, regulatory documentation, and data integrity practices.
Experience Required
2–6 years of hands-on experience in regulated small molecule bioanalytical laboratory environments
Proven experience in method development, validation, and study sample analysis
Experience in BA/BE studies under GLP/GCP compliance
Prior experience in a Bioanalytical CRO laboratory is preferred
Educational Qualification
Master’s degree in Pharmaceutics or related Life Sciences discipline from a recognized university – Mandatory
Key Responsibilities
Bioanalytical Study Execution
Perform bioanalytical experiments including sample processing for method development, method validation, and study sample analysis
Conduct BA/BE studies in compliance with approved protocols, SOPs, and STPs
Ensure adherence to GLP/GCP regulatory standards
Method Development & Validation
Develop and validate analytical methods for small molecule analysis
Prepare Study Test Procedures (STP), Method Validation (MV) protocols, and sample analysis protocols
Troubleshoot analytical challenges and ensure method robustness
Instrumentation & Technical Support
Operate and maintain analytical instruments such as LC-MS/MS and HPLC
Coordinate with maintenance teams for equipment calibration, preventive maintenance, and troubleshooting
Ensure instrument compliance and documentation readiness for audits
Data Documentation & Compliance
Record experimental data in compliance with ALCOA++ data integrity principles
Maintain official documentation and ensure timely response to QC/QA observations
Minimize audit findings through rigorous documentation and compliance discipline
Scientific & Cross-Functional Engagement
Participate in scientific discussions related to project execution
Communicate results effectively to internal stakeholders
Identify risks proactively and implement mitigation strategies
Core Competencies
Scientific Competencies
Strong understanding of small molecule bioanalysis
Scientific problem-solving and logical troubleshooting ability
Curiosity-driven learning mindset
Ability to interpret complex bioanalytical data
Technical Competencies
Expertise in LC-MS/MS and HPLC-based assays
Accurate execution of experiments with minimal deviations
Strong project management and organizational skills
Documentation & Compliance
Strict adherence to ALCOA++ principles
Strong written communication skills
Timely and accurate response to quality and audit requirements
Why This Role Matters
This role directly supports translational and clinical research programs by ensuring high-quality bioanalytical data generation. It contributes to regulatory submissions, clinical development milestones, and global pharmaceutical research initiatives.
Equal Opportunity Employer
Syngene International Ltd. is committed to providing equal employment opportunities to all qualified individuals. Employment decisions are based on merit and business needs, without discrimination based on legally protected characteristics. Reasonable accommodations are provided where required.
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