Key Responsibilities:
- Perform routine and non-routine chemical analysis using analytical instruments.
- Operate and maintain instruments such as HPLC, GC, UV-Vis Spectrophotometer, and FTIR.
- Prepare reagents, standards, and solutions required for testing.
- Conduct method development and validation as per regulatory guidelines.
- Analyse and interpret data, and prepare reports with accuracy.
- Ensure compliance with GMP, GLP, and safety protocols.
- Maintain proper documentation as per SOPs.
- Investigate out-of-specification (OOS) results and deviations.
- Support audits and inspections by regulatory authorities.
- Coordinate with production and QA teams for quality-related issues.
Required Skills:
- Strong knowledge of analytical techniques and instrumentation.
- Familiarity with GMP/GLP guidelines.
- Good documentation and reporting skills.
- Attention to detail and accuracy.
- Problem-solving and analytical thinking.
- Basic computer knowledge (MS Office, lab software).
Preferred Skills:
- Experience in pharmaceutical or chemical industry.
- Knowledge of method validation and stability studies.
- Exposure to regulatory requirements (e.g., FDA, WHO).
Key Competencies:
- Analytical mindset
- Time management
- Team collaboration
- Quality focus
Job Type: Full-time
Pay: ₹15,000.00 - ₹20,000.00 per month
Work Location: In person
