Analyst Job at Syngene for M Pharma Graduates | Apply
Syngene International Ltd. is hiring a Sr. Research Associate / Sr. Executive / Sr. Analyst for the Small Molecule Bioanalytical Research Laboratory in Bangalore, India. This role offers an exciting opportunity to work on regulated bioanalytical studies, including method development, validation, and sample analysis. If you are detail-oriented, scientifically curious, and committed to excellence, join Syngene Careers and contribute to world-class pharmaceutical and biotechnology research.
Job Details
- Job Position: Analyst – Small Molecule Bioanalytical Research Laboratory (BRL)
- Location: Bangalore, India
- Department: Discovery Services
About the Company
Syngene International Ltd. is a global integrated research, development, and manufacturing solutions company serving pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. With over 4,500 scientists and 1.9 million sq ft of specialist facilities, Syngene delivers robust science, data management, and quality manufacturing to accelerate innovation for biotech companies and global multinationals including GSK, Amgen, Baxter, and Bristol-Myers Squibb. The Analyst job here entails contributing to such innovative efforts.
Explore Syngene Careers to join a company that combines scientific excellence with innovative solutions to improve time-to-market and reduce the cost of drug development.
Job Description
The Analyst is a M Pharma Job will perform regulated bioanalytical studies for small molecules, including BA/BE studies, method development, method validation, and study sample analysis. The role ensures compliance with SOPs, regulatory standards (GCP/GLP), and supports accurate documentation and data reporting. The position reports to the Project Leader / Group Leader of the Small Molecule Bioanalytical Laboratory, which focuses on analyst job tasks within the field.
Key Responsibilities
- Conduct bioanalytical experiments for method development, validation, and study sample analysis.
- Prepare STP, MV protocols, and sample analysis protocols.
- Coordinate with maintenance for equipment and instrument issues (LC-MS/MS, HPLC, etc.).
- Document all data following regulatory and company standards (ALCOA++).
- Ensure compliance with GCP/GLP and internal quality standards.
- Participate in project discussions and provide scientific input, bringing analyst job proficiency.
Educational Qualification
Master’s degree in Pharmaceutics
Experience and Skills
- Minimum 3 years of experience in regulated small molecule bioanalysis.
- Hands-on experience in bioanalytical experiments.
- Experience in a Bioanalytical CRO lab is an advantage.
