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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

Job Description

To perform calibration of the analytical instruments as per calibration schedule

Follow the standard practices cGLP during lab experiments

Cleaning verification method development

API method evaluation and verification

API solubility study assessment

Column numbering and management

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

TRF entries in common portal for tracking management

Ensure use of Personal Protective Equipment & attend EHS training & send waste to concerned person & comply EHS requirements.

Follow GxP (GMP, GDP, GLP) for all processes.