Syngene International Ltd. is a leading contract research and manufacturing company (CRAMS) offering integrated drug discovery, development, and manufacturing services to the global pharmaceutical, biotechnology, nutrition, animal health, and specialty chemical industries.

With over 4500+ scientists and a global reputation for quality, compliance, and innovation, Syngene partners with top pharmaceutical companies like GSK, Merck KGaA, Amgen, and Bristol-Myers Squibb.

Visit the official website: https://www.syngeneintl.com

Open Positions: Executive – Bioanalytical

Job Title: Research Associate / Executive / Analyst
Department: Clinical Development – Small Molecule Bioanalytical Laboratory
Company: Syngene International Ltd.
Location: Bangalore, Karnataka, India – 560100
Industry: Pharmaceutical / Biotechnology / Bioanalytical Research
Job Posting Date: 4 August 2025

Job Role Overview

The selected candidate will work in the Small Molecule Bioanalytical Laboratory as part of the Clinical Development team. The role involves method development, method validation, and sample analysis under regulated environments.

This position is ideal for candidates with a background in pharmaceutics or related life sciences and at least 1 year of experience in regulated bioanalytical laboratories.

Key Responsibilities

Perform sample processing for method development, validation, and study analysis

Prepare documents such as:

Study Sample Analysis Protocol (SAP)
Method Validation Protocol (MVP)
Standard Testing Protocol (STP)

Operate and troubleshoot instruments like LC-MS/MS and HPLC
Ensure data recording and documentation follow ALCOA++ and GLP/GCP guidelines
Participate in scientific discussions and regulatory compliance reviews

Required Qualifications

Education: M.Pharm / M.Sc in Pharmaceutics or relevant Life Sciences
Experience: Minimum 1 year in regulated small molecule bioanalysis
Technical Skills: Hands-on with LC-MS/MS, HPLC, documentation standards, regulatory compliance
Location: Bangalore, Karnataka, India

Preferred Skills

Experience working in a bioanalytical CRO environment
Strong communication and documentation skills
Ability to troubleshoot instruments and plan risk mitigation steps
Understanding of GCP, GLP, and regulatory requirements for clinical studies

Core Competencies

Scientific thinking – Ability to understand and interpret bioanalytical problems
Technical execution – Skill in performing and documenting complex lab protocols
Regulatory compliance – Knowledge of FDA, EMA, ICH guidelines in clinical development
Data integrity – Familiarity with ALCOA++ principles and clean documentation practices

Job Benefits

Opportunity to work with global clients and cutting-edge technologies
Access to advanced instrumentation and learning opportunities
Competitive compensation in the pharmaceutical research and development sector
Work environment aligned with international clinical research standards

Equal Opportunity Employer

Syngene is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, gender, sexual orientation, disability, or any other protected status.

How to Apply

Interested candidates can apply through the official careers page:

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