Senior Executive

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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

• Analysis of stability sample, finished product and related documentation as per cGMP.

• Responsible for only run the method in the KF Instrument , Dissolution Instrument , UV Instrument , HPLC, does not access to change the method, report format and method configuration.

• Responsible to perform Dissolution testing, KF apparatus, IR, UV, Friability, DT, pH and physical testing etc.

• Maintenance of stability incubators & chamber.

• Preparation of stability monthly planner.

• Receipt/Inward/Storage of QC samples.

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

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

• Any additional responsibility assigned by section head.

• Maintenance of Bin Card of chemical store.

• Follow of GLP / GMP requirements.  

• maintain QC Laboratory Records. (Like Laboratory note Book, COA and SSR etc.).

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