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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

Follow GLP, GDP and Data Integrity practices while working in laboratory

Ø To perform sampling of raw material and packaging materials as per SOP.

Ø Routine analysis of Raw materials, packaging materials, In-process, finished products,

Cleaning swabs and Stability samples.

Ø To perform preventive maintenance and calibration of the analytical instruments as per

calibration schedule.

Ø Preparation of technical documents like SOPs, specifications, COA, STP, Validation

protocols/reports, Transfer protocols/reports etc.

Ø Archival and retrieval of system documents i.e. Instrument logbooks, Registers etc.

Ø Validation and Verification of analytical methods.

Ø Lab temperature monitoring.

Ø Follow GxP (GMP, GDP etc.) for all processes.

Reporting of analytical data and submit for review and release.

Ø Maintain hygienic condition in respective department.

Ø Standard, column and chemicals Management.

Ø Balance and pH meter/conductivity meter verification and calibration.

Ø Ensure use of Personal Protective Equipment & attend EHS training & send waste to

concerned person & comply EHS requirements.