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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

·    Analyst who is able to performed analysis of AMV/AMT, finished product, stability samples and raw materials as per cGMP and USFDA requirement.

·    Able to prepare protocol and report and other related documentation as per GDP.

·    Should have hands-on experience on HPLC, GC, FTIR, Dissolution Test apparatus, KF, LC-MS/MS, AAS, Malvern PSD analyser etc.

·    Should have sound knowledge of cGMP, GLP, GDP, ICH and ALCOA++

·    Receipt/Inward/Storage of QC samples and Disposition of sample after analysis.

·    Concurrent documentation of analytical records and storage of raw data, online entries in Instrument/ Equipment’s usage logbooks.

·     Instant reporting in case of any deviation, incident, OOT or OOS to Section Head/ Head QC.

·       Any additional responsibility assigned by section head.

·      Implementation of GLP / GMP requirements. 

·      To control and maintain QC Laboratory Records. (Like Laboratory, note Book and COA etc.).

·       Support to site DICO (Data Integrity Compliance Officer) for monitoring and implementation of actions related to Data Integrity awareness at site.