Syngene International Require Bioresearch Laboratory Scientist

Syngene International Ltd. is an innovation-focused global discovery, development, and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries worldwide. Syngene’s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife. Its innovative culture is driven by the passion of its 4240- a strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market, and lower the cost of innovation.

Post : Scientist - Bioresearch Laboratory

Job Description
• 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.

Candidate Profile
• Masters in Pharmaceutics or other related life sciences from a reputed university.
• Hands-on experience in small molecule regulated bioanalytical experiments
• People leadership experience
• Experience with working for a Bioanalytical CRO lab will be an added advantage.

Core competencies required for the role
• Scientific :
o Brings a creative and an innovative advantage to projects
o Is curious, eager to learn and make a difference
o Thinks scientifically and understands the problem statement in assigned programs/assays
o Publishes posters, papers and articles regularly
• Technical
o Conducts/plans experiments without errors and gaps
o Reports/analyzes data punctually and communicates effectively
o Troubleshoots and investigates logically (is able to defend the logic behind experimental results)
o Is able to forecast risks and make mitigation plans ahead of time
o Has good organizational, project management skills
• Documentation
o Records data as per ALCOA++ policy
o Pays attention to detail
o Is punctual in responding to QC and QA reports
o Displays minimal audit finding index
o Writes clearly and concisely with English skills at >B+

Additional Information
Qualification : MSc, M.Pharm
Location : Bangalore
Division : Discovery Services
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 28th February 2026