MSc Pharmaceutics Jobs at Syngene | Apply Now for Executive- Bioanalytical Position
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.
About 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.
JOB DESCRIPTION
Position: Executive – Bioanalytical
Date: 4 Aug 2025
Location:
Bangalore, KA, IN, 560100Custom Field 1: Development Services
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
Education and Experience
Education: Master’s in Pharmaceutics or other related life sciences from a reputed university.
Industry Experience
- Minimum of 1 year of experience in regulated small molecule bioanalysis
- Hands-on experience in small-molecule-regulated bioanalytical experiments
Exposure and experience
Experience working for a Bioanalytical CRO lab will be an added advantage.
Core competencies required for the role
Scientific:
- Brings a creative and 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 (can defend the logic behind experimental results)
- Can forecast risks and make mitigation plans ahead of time
- Has good organizational, project management skills
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 to the Project Leader / Group Leader, Small Molecule Bioanalytical Laboratory, and is a full-time position based out of Bangalore, India.
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+
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 the 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.
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