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Executive

Syngene
Syngene
1-4 years
preferred by company
10 Jan. 26, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Executive / Research Associate / Analyst – Small Molecule Bioanalytical Research

Division: Discovery Services
Location: Bangalore, Karnataka, India (560100)
Employment Type: Full-time
Job Grade: Level 9-I
Date Posted: January 12, 2026

About Syngene International

Syngene International Ltd. is a leading integrated research, development, and manufacturing services organization supporting global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries. With a workforce of over 4,500 scientists and world-class infrastructure spanning discovery, development, and manufacturing, Syngene partners with innovative biotech firms and multinational pharmaceutical companies to accelerate scientific advancement while ensuring robust data integrity, IP security, and regulatory compliance.

Job Overview

Syngene is seeking a motivated Executive / Research Associate / Analyst to join its Small Molecule Bioanalytical Research Laboratory within Translational and Clinical Research. This is a hands-on laboratory role focused on the execution of regulated bioanalytical studies, including method development, method validation, and study sample analysis for small molecules.

The position requires strong technical expertise in bioanalysis, a solid understanding of regulatory guidelines, and a high commitment to data integrity, quality, and compliance. The role reports to the Project Leader or Group Leader and is based at Syngene’s Bangalore facility.

Key Responsibilities

Bioanalytical Operations

  • Perform bioanalytical experiments including sample processing for method development, method validation, and study sample analysis in accordance with approved protocols

  • Execute BA/BE studies while ensuring strict compliance with SOPs and STPs

  • Prepare study-related documentation including STPs, method validation protocols, and sample analysis protocols

  • Accurately document experimental data and maintain official laboratory records

Instrumentation & Compliance

  • Operate and support troubleshooting of bioanalytical instruments such as LC-MS/MS and HPLC

  • Coordinate with maintenance and engineering teams to resolve equipment or utility-related issues

  • Ensure all activities comply with applicable GCP and GLP regulatory guidelines

  • Adhere to ALCOA++ principles for data integrity and regulatory documentation

Scientific Contribution

  • Participate in project-level scientific discussions and provide technical input

  • Analyze, interpret, and report data clearly and in a timely manner

  • Identify potential risks in experiments and proactively develop mitigation strategies

Education & Experience

Educational Qualification

  • Master’s degree in Pharmaceutics or a related life sciences discipline from a recognized university

Experience Required

  • 1–4 years of hands-on experience in regulated small molecule bioanalytical experiments

  • Prior experience working in a Bioanalytical CRO laboratory is highly desirable

Core Competencies

Scientific & Technical Skills

  • Strong understanding of small molecule bioanalysis and regulated laboratory practices

  • Ability to independently plan and execute experiments with minimal errors

  • Logical troubleshooting and strong scientific reasoning to defend experimental outcomes

  • Proficiency in data analysis, reporting, and risk assessment

Documentation & Quality

  • Excellent attention to detail and adherence to ALCOA++ documentation standards

  • Timely and accurate response to QC and QA observations

  • Consistent performance with minimal audit findings

  • Strong written communication skills in English, with clear and concise documentation

Professional Attributes

  • Curious, innovative, and eager to learn

  • Strong organizational and project management capabilities

  • Effective communicator and collaborative team contributor

Equal Opportunity Statement

Syngene International Ltd. is an equal opportunity employer and is committed to creating an inclusive workplace. Employment decisions are made without regard to age, race, gender, disability, religion, sexual orientation, or any other characteristic protected by applicable laws. Reasonable accommodations are provided for qualified individuals with disabilities.

About Discovery Services

This role is part of Syngene’s Discovery Services division, which supports early-stage research and translational science for global clients across multiple therapeutic areas.