Senior Research Associate-AD

Piramal Pharma

Ahmedabad, GJ, India6d ago

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Key details

Location
Ahmedabad, GJ, India
Work style
Onsite
Level
Mid level
Job type
Full-time
Function
Science & Research
Focus area
other
Posted
6d ago

Skills

calibrationgmp

About the role

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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

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.

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