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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

1.    Analysis of Finished products, In-process, Hold time, Raw Materials, stability samples and related documentation as per cGMP.

2. Preparation of the Analytical Method transfer/Validation/Verification protocol and reports.

3. Execution of Analytical Method transfer/Validation/Verification activity for new Projects.

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

5.  Any additional responsibility assigned by section head.

6.   Implementation of GLP / GMP requirements. 

7.   To control and maintain QC Laboratory Records. (Like Laboratory notebook, Chromatograms, and COA etc.).

8.   Operations with ENSUR and Track wise. (Carry out OOS, OOT, Lab Investigation report.)

9.   Preparation and Standardization of volumetric solutions/ Reagents/ Indicator solution preparation as and when required.

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

11.      Analysis of Vendor Approval samples or RLD Samples.