Analytical Development for Pharma Industry

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