Job Description

Key Responsibilities:


Develop and validate analytical methods for raw materials, intermediates, and

finished products using HPLC, GC, UV, FTIR, and other analytical techniques.


Perform stability studies as per ICH guidelines and prepare related documentation.


Conduct routine analysis to support formulation development and process

optimization.


Prepare and review analytical method development and validation protocols and

reports.


Ensure compliance with cGMP, GLP, and internal SOPs during all analytical activities.


Maintain laboratory instruments and calibration logs; handle troubleshooting of

equipment.


Document results accurately in lab notebooks, software systems, and reports.


Coordinate with cross-functional teams including QA, QC, F&D, and Regulatory

Affairs.


Assist in technology transfer and support scale-up activities.


Prepare analytical documentation for regulatory submissions (ANDA, CTD, etc.).

Key Skills Required:


Hands-on experience with HPLC, GC, UV, IR, Dissolution apparatus, etc.


Good understanding of ICH guidelines, regulatory expectations, and validation

practices


Sound knowledge of GMP/GLP documentation practices


Ability to handle multiple projects and meet deadlines


Proficiency in analytical software (e.g., Empower, Chromeleon) is a plus


Strong communication and teamwork skills

Qualication

M.Sc. (Analytical Chemistry / Organic Chemistry) / B. Pharm / M. Pharm

Job Type: Full-time

Pay: ₹30,000.00 - ₹40,000.00 per month

Schedule:

Day shift
Experience:

Analytical Development: 2 years (Preferred) Method Development: 1 year (Preferred) Method Validation: 1 year (Preferred) Analytical Method Validation: 1 year (Preferred) HPLC: 1 year (Preferred) GC: 1 year (Preferred) UV: 1 year (Preferred) IR: 1 year (Preferred)
Location:

Ahmedabad, Gujarat (Preferred)
Work Location: In person