Senior Research Associate - AD

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Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.

Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Senior Research Associate - AD

Job Description

 Routine analysis of formulation samples
 Calibration of analytical instruments
 Stability study of lab batches
 Preparation of test procedure, development reports
 Review of routine analytical activities (Peer review)

Role: It includes the brief description of the work

• Routine analysis of formulation samples
• Calibration of analytical instruments
• Stability study of lab batches
• Preparation of test procedure, development reports
• Review of routine analytical activities (Peer review)

Job Description: It includes the job duties and responsibilities of the work

• To perform calibration of the analytical instruments as per calibration schedule
• Follow the standard practices cGLP during lab experiments
• Cleaning verification method development and validation
• API method evaluation and verification
• API solubility study assessment
• Method Development for drug product formulation
• Routine analysis of development samples and lab stability samples
• Method verification of different analytical methods
• Reporting of analytical data and submit for review and release
• ARF release of raw material and packaging material
• Preparation of test procedures for routine development analysis
• Follow in-house compliance system
• Maintain hygienic condition in respective department
• Column Management
• TRF entries in common portal for tracking managment

• Ensure use of Personal Protective Equipment & attend EHS training & send waste to concerned person & comply EHS requirements. v Follow GxP (GMP, GDP, GLP, DI) for all processes.