Latest Life Science Jobs at Syngene | Apply Now for Executive – Bioanalytical  Role

Latest MSc Life Science Jobs at Syngene | Apply Now for Executive – Bioanalytical  Role

Are you a skilled life sciences professional seeking your next career move? Syngene International Ltd. is offering an exciting Small Molecule Bioanalysis Job at its world-class facility in Bangalore. This full-time role is ideal for candidates with hands-on experience in regulated bioanalytical studies, including method development, validation, and sample analysis. Join a global leader in pharmaceutical R&D and contribute to cutting-edge research that accelerates innovation worldwide.

Executive – Bioanalytical

Date: 4 Aug 2025

Location: Bangalore, KA, IN, 560100

Custom Field 1: Development Services

JOB DESCRIPTION

Designation: Research Associate/ Executive/ Analyst, Small Molecule Bioanalytical Research Laboratory, Clinical Development

Job Location: Bangalore, India

Reporting to: Group Leader of Small Molecule Bioanalytical Laboratory

Job Grade: Level 9-I

The Company

Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development, and manufacturing solutions company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngene’s 4500+ scientists offer both the skills and capacity to deliver great science, robust data management and IP security, and quality manufacturing at speed, to improve time-to-market and lower the cost of innovation. With a combination of 1.9 Mn sq ft of specialist discovery, development and manufacturing facilities, as well as dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb and Herbalife, Syngene works with biotech companies pursuing leading edge science as well as multinationals including GSK and Merck KGaA.

The Role

The Research Associate/ Executive/ Analyst for the Small Molecule Bioanalytical Laboratory is a technical role responsible for conducting BA/BE studies in the laboratory. Job responsibilities include performing critical method development and validation programs, technical and regulatory compliance of all studies.

This role requires an individual with a robust background in pharmaceutics, or other related life sciences, coupled with extensive experience in the bioanalytical field, particularly within small molecule bioanalysis.

This role demands an individual with a strong commitment to compliance, integrity, and excellence in bioanalytical research, particularly in small molecule analysis. The role reports into the Project Leader / Group Leader, Small Molecule Bioanalytical Laboratory and is a full-time position based out of Bangalore, India.

Key Responsibilities of the Role:

• Perform the bioanalytical work including sample processing for method development, method validation and study sample analysis as per the protocol in compliance with SOPs, STPs.
• Prepare STP, MV protocol and study sample analysis protocol.
• Coordinate with maintenance department for any problems related to utilities and equipment / instrument (e.g. LC-MS/MS, HPLC, etc) failures.
• Document data generated, entries in official documents.
• Ensure all studies adhere to regulatory guidelines and expectations set by GCP/ GLP.
• Participate in all discussions on project-specific scientific details.

Education and Experience

Education: Masters in Pharmaceutics or other related life sciences from a reputed university.

Industry Experience

• Minimum of 1 years of experience in regulated small molecule bioanalysis
• Hands-on experience in small molecule regulated bioanalytical experiments

People leadership experience

NA

Exposure and experience

Experience with working for a Bioanalytical CRO lab will be an added advantage.

Core competencies required for the role

Scientific:

• Brings a creative and an innovative advantage to projects
• Is curious, eager to learn and make a difference
• Thinks scientifically and understands the problem statement in assigned programs/assays
• Publishes posters, papers and articles regularly

Technical

• Conducts/plans experiments without errors and gaps
• Reports/analyzes data punctually and communicates effectively
• Troubleshoots and investigates logically (is able to defend the logic behind experimental results)
• Is able to forecast risks and make mitigation plans ahead of time
• Has good organizational, project management skills

Documentation

• Records data as per ALCOA++ policy
• Pays attention to detail
• Is punctual in responding to QC and QA reports
• Displays minimal audit finding index
• Writes clearly and concisely with English skills at >B+

APPLY ONLINE HERE

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