Cipla - FADL - On Teamlease Payroll

Cipla; Mumbai; On-site; INR 450,000 - 600,000; Full time

Job summary

Cipla in Mumbai is seeking an Associate - Formulation ADL to perform analytical testing of formulation samples and support method development, validation, and transfer activities. You will operate instruments like HPLC, UV, dissolution apparatus, and GC, while ensuring GLP/GMP compliance and data integrity.

You will prepare reagents and laboratory records, assist in stability studies, and coordinate with formulation, QC, and regulatory teams to meet project requirements.

Qualifications

• Solid understanding of analytical testing and documentation.
• Familiarity with GLP/GMP requirements and data integrity.

Responsibilities

• Perform analytical testing of formulation samples as per approved methods.
• Support method development, validation, and transfer activities.
• Operate HPLC, UV, Dissolution Apparatus, and GC.
• Prepare reagents, solutions, and records per GLP/GMP.
• Maintain laboratory documentation and data integrity.
• Assist in stability studies and sample analysis.
• Coordinate with formulation, QC, and regulatory teams.

Skills

Good documentation

Communication skills

cGMP knowledge

GLP/GMP understanding

Tools

HPLC

Dissolution apparatus

UV spectroscopy

GC

Job description

Job Role: Associate - Formulation ADL

Key Responsibilities:

• Perform analytical testing of formulation samples as per approved methods.
• Support method development, method validation, and method transfer activities.
• Operate analytical instruments such as HPLC, UV, Dissolution Apparatus, and GC.
• Prepare reagents, solutions, and laboratory records as per GLP/GMP requirements.
• Maintain analytical documentation and ensure data integrity.
• Assist in stability studies and sample analysis.
• Coordinate with formulation, QC, and regulatory teams for project requirements.
• Ensure compliance with laboratory safety and quality standards.

Skills Required:

• Knowledge of HPLC, Dissolution, UV spectroscopy.
• Understanding of analytical method development and validation.
• Good documentation and communication skills.
• Knowledge of cGMP and regulatory guidelines.