This role has closed. Piramal Pharma has taken the posting down.
hirly last saw it live on 25 September 2026. See similar open roles below, or browse the live board.
Piramal Pharma
Research Associate-R&D
Ennore, TN
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hirly's read of this role
- Seniority
- Mid level
- Country
- US
- Work mode
- On-site / unstated
- First seen by hirly
- 24 Sept 2026
Derived automatically from the posting.
the posting
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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
Research Associate-R&D Job Description
To execute the analysis in lab independently under the guidance of the supervisor, responsible to maintain lab records and work place. Responsibilities :-
- To support NMR analysis for R&D routine sample under the supervision of senior analytical scientist.
- Perform wet chemical analysis like LOD, ROI Moisture content, & melting points
- Analysis using Spectroscopic technique like IR, UV-VIS spectrophotometer.
- Calibration of instrument like Analytical balance, pH meter, KF tiltrotor, melting point HPLC, GC UV-VIS spectrophotometer and IR as per SOP.
- Sampling of raw materials, intermediates, and finished products.
- Routine sample analysis by HPLC and GC individually under supervision of senior analytical scientist.
- Strict adherence to cGMP & GLP norms and safety rules of the factory.
- Qualification: M.Sc. – Chemistry
- Experience: 1-3 Years experience