Syngene International is hiring for the position of Senior Analyst in its Development Services division at Bangalore. The opening is in the Early Phase GMP – Analytical Development department. Candidates with an MSc or M.Pharm qualification and 1 to 6 years of experience can apply.
Job Details
| Particulars | Details |
|---|---|
| Company | Syngene |
| Job Title | Senior Analyst |
| Division | Development Services |
| Department | Early Phase GMP – Analytical Development |
| Job Location | Bangalore, Karnataka |
| PIN Code | 560099 |
| Experience | 1–6 Years |
| Qualification | MSc / M.Pharm |
| Job Posting Date | 7 November 2026 |
Job Responsibilities
Selected candidates will be responsible for the following activities:
- Perform analysis of raw materials, in-process materials, intermediates, and finished products.
- Handle analytical instruments, including HPLC, GC, UV, KF, and FTIR.
- Perform sampling of raw materials, intermediates, and finished products.
- Handle Quality Management System (QMS) activities.
- Perform instrument calibration and qualification.
- Maintain the laboratory as per Good Manufacturing Practice (GMP) requirements.
- Manage reserve samples.
- Conduct stability analysis.
- Participate in validation activities.
Eligibility and Qualifications
- Educational Qualification: MSc or M.Pharm.
- Work Experience: 1 to 6 years.
- Candidates should have experience relevant to analytical development and laboratory activities.
Required Technical Skills
Candidates should have relevant knowledge or experience in:
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- HPLC
- Gas Chromatography (GC)
- UV Spectrophotometry
- Karl Fischer (KF)
- FTIR
- Raw material and finished product analysis
- In-process and intermediate analysis
- Instrument calibration and qualification
- GMP laboratory practices
- Quality Management System (QMS)
- Stability analysis
- Validation activities
- Sampling and reserve sample management
Safety and GMP Compliance Expectations
Syngene emphasizes safety, quality, and operational discipline. Employees are expected to:
- Follow workplace safety procedures and EHS requirements.
- Maintain compliance with company quality standards.
- Complete mandatory training related to data integrity, health, and safety.
- Follow laboratory safety protocols and GMP requirements.
- Contribute to safe laboratory operations and compliance practices.
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