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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

Issuance and control of documents. (e.g. SOPs, BMR, BPR, Formats, Logbooks and LNBs).

Management of Archival and Retrieval of documents.

Updating of Logbooks related to QMS documents (i.e. change control, deviation, OOS etc).

Monitoring of temperature for retention sample storage.

Participation in audit for arrangement of documents pre-audit and timely document availability during audits.