Syngene is inviting applications for the role of Senior Analyst in the Early Phase GMP (Analytical Development) department at Bangalore. This opportunity is suitable for M.Sc. or M.Pharm candidates with hands-on experience in analytical development, QC laboratory practices, method validation, and instrument-based analysis.
Job Details
| Company | Syngene |
| Position | Senior Analyst |
| Department | Early Phase GMP (Analytical Development) |
| Location | Bangalore, KA, IN, 560099 |
| Work Mode | On-site |
| Qualification | M.Sc. / M.Pharm (Analytical Chemistry / General Chemistry) |
| Experience | 1 to 6 years |
Job Description
The Senior Analyst will perform analytical reference standard qualifications and characterizations, method validations and verifications, related documentation, and analysis of raw materials, packing materials, intermediates, APIs, and finished products.
The role requires working in a QC laboratory environment while following Good Laboratory Practices, safety protocols, Syngene quality standards, and EHSS requirements.
Key Responsibilities
- Follow Good Laboratory Practices (GLP) while working in the QC laboratory.
- Maintain and clean assigned laboratory instruments.
- Use required safety apparel while sampling, analyzing, and working in the laboratory.
- Carry out analysis of validation samples as per approved protocols.
- Initiate laboratory incidents and deviations as required.
- Prepare calculation sheets and draft reports.
- Ensure proper disposal of samples after analysis.
- Perform any additional duties assigned by the HOD or Section Head.
- Analyze intermediates, finished products, and working standard qualifications as per specifications.
- Verify and review instrument usage logs periodically and ensure labeling compliance as per SOPs.
- Prepare protocols and observation data sheets.
- Work with analytical techniques including HPLC, GC, KF/KFC, IR, UV, LC-MS, GC-MS, IC, and ICP-OES/ICP-MS.
- Utilize Chromeleon data management software and LIMS effectively.
- Ensure compliance with Syngene safety policies and EHSS requirements.
Qualification
- M.Sc. / M.Pharm in Analytical Chemistry or General Chemistry.
- Hands-on experience with analytical techniques such as HPLC, GC, KF/KFC, IR, UV, LC-MS, GC-MS, IC, ICP-OES/ICP-MS, DSC, and TGA.
- Knowledge of Chromeleon data management application and LIMS will be an added advantage.
Experience
Candidates should have 1 to 6 years of relevant experience.
Safety and Compliance Expectations
- Overall adherence to safe practices and procedures for self and aligned teams.
- Contribute to the development of procedures, practices, and systems that ensure safe operations and compliance with company integrity and quality standards.
- Drive a corporate culture that promotes an Environment, Health and Safety (EHS) mindset and operational discipline at all times.
- Ensure safety of self, team members, and laboratory/plant by adhering to safety protocols and EHS requirements.
- Ensure completion of all mandatory trainings related to data integrity, health, and safety within stipulated timelines.
- Ensure compliance with Syngene quality standards at all times.
- Hold self and team accountable for achieving safety goals.
- Govern and review safety metrics periodically.
How to Apply
Interested and eligible candidates can apply online through the official Syngene careers link given below.
