Posted 29 days ago
Senior Research Associate-AD
AI Summary
Performs routine analysis of formulation samples, calibrates analytical instruments, conducts stability studies, develops and verifies analytical methods, and maintains compliance with GxP standards in a pharmaceutical R&D lab.
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Division
Piramal Pharma SolutionsPiramal 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-ADJob 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)
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
Area and Milli-Q monitoring
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.v Follow GxP (GMP, GDP, GLP) for all processes.
Skills
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