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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
Performing analytical and development studies related to oral solid drug products. Position requires expertise in solid state screening, analytical characterization, and method development while demonstrating strong analytical thinking and a commitment to quality and compliance.
Design and perform screenings of polymorphs, salts, and co-crystals (including hydrates and solvates) of Active Pharmaceuticals Ingredients through crystal engineering principles by utilizing different screening (crystallization) methods.
- Characterization of polymorphs, co-crystals, salts and novel polymorphs, and their data interpretation of solid state techniques such as PXRD, DSC, TGA, IR, Polarized microscopy, Hot stage microscopy and RVC.
- Method developments and Method Validations of analytical methods as per ICH guidelines by using Powder X-Ray Diffraction Techniques for both drug product as well as drug substance.
- Calibration of the analytical instruments and preventive maintenance as per calibration/maintenance schedule in solid-state characterization team.
- Experimental physico-chemical properties determination like pKa and Log P by titration and spectroscopic techniques.
- Perform Solubility study and Dissolution studies as per guideline.
- Perform day-to-day routine laboratory activities in solid-state characterization team.
- Interpretation of analytical characterization results.
- Qualification of instruments and related CSV activities.
- Communication with supplier/vendors for Instrument maintenance and columns/chemicals/spare parts inquiry.
- Provide project updates to clients through emails, telecom communications and by PowerPoint presentations.
- Ensure/Review standard practices cGLP during lab experiments.
Master of Pharmacy (M.Pharm)
