Syngene Hiring Senior Analyst-Development Services Role | Apply Online
Looking for a Quality Control Job in the pharmaceutical industry? Syngene Careers has announced an exciting opportunity for the position of Senior Analyst in the Early Phase GMP – Analytical Development department at its Bangalore facility. This Quality Control Job is ideal for candidates with M.Pharm (Analytical) qualifications who are eager to work with advanced analytical techniques and GMP laboratories.
About the Company
Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.
At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety on par with business performance, with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in letter and spirit.
Job Details
| Company | Syngene |
| Job Title | Senior Analyst |
| Department | Early phase GMP – Analytical Development |
| Location | Bangalore, KA, IN, 560099 |
| Qualification | M Sc / M Pharma (Analytical/General Chemistry) |
| Experience | Foundational |
Job Description
The role involves performing analytical method validations and related documentation, along with analysis of RM, PM, Intermediates, API, and Finished products. The Senior Analyst will conduct chromatographic and non-chromatographic analysis using qualified techniques as per approved specifications, protocols, and procedures. Responsibilities include interpretation of analytical data, documentation in compliance with cGMP and GDP, timely reporting of results, and supporting method transfers and validation activities for multiple client projects.
Key Responsibilities
- Perform Chromatographic and Non-chromatographic analysis for Drug substances, Drug products, Intermediates, and Excipients.
- Interpret data from analytical instruments and submit completed documents for review within the established window.
- Record analytical observations in data sheets, logbooks, LIMS, and ELN software.
- Perform validation activities and method transfers for multiple client projects.
- Ensure timely reporting and investigation of events or deviations.
- Conduct instrument calibration and preventive checks for laboratory instruments.
- Prepare Certificates of Analysis and reports for Analytical Method Validation and Transfer.
- Actively participate in client and regulatory audits and ensure compliance with cGMP and GDP.
Safety & Compliance Expectations
- Overall adherence to safe practices and procedures of oneself and aligned teams.
- Contribute to development of procedures and systems ensuring safe operations and compliance.
- Drive an environment, health, and safety (EHS) mindset and operational discipline.
- Ensure completion of mandatory trainings related to data integrity, health, and safety.
- Compliance to Syngene’s quality standards at all times.
- Govern and review safety metrics from time to time.
Eligibility Criteria
- Educational Qualification: M Sc / M Pharma (Analytical/General chemistry)
- Experience: Foundational
Technical / Functional Skills
- Knowledge of analytical techniques such as HPLC/GC, KF/KFC, IR/UV, LC-MS, GC-MS, IC, ICP-OES/ICP-MS, DSC, TGA.
- Familiarity with Chromeleon data management application.
- Working knowledge of LIMS, ELN, and LMS software.
Behavioral Skills
- Adaptive learner.
- Effective communication skills.
- Organization and ability to balance work and life.
- Good time management abilities.
