Technical Staff

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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

• responsible for proper dispensing and issuence  of Raw materials.
• Responsible for handling of retest and expired materials.
• Responsible for monitoring the temperature and RH related activity.
• Responsible for timely and correct material dispensing and issuance to production for manufacturing.
• Responsible for coordination with production for timely batch requirement and arrangement of in process container (IPC) and planning for timely batch releases.
• Responsible for coordination with QA for timely execution of Batch Manufacturing Record
• Responsible for timely preparation of Dispensing Label and potency calculation in BMR.
• Responsible for maintaining routine housekeeping in warehouse areas as per cGMP norms.
• Responsible for correct Data entry in SAP system.
• Responsible for compliance of cGMP, preparation of various regulatory and statuary audits.
• Responsible for training to workman time to time.
• Responsible for timely preparation of cGMP and other legal documents and its authorization as per requirement.
• Responsible for coordinate with Planning/Purchase/QC/Production for minimize inventory of Raw materials to avoid slow moving/non-moving and near expiry inventory.
• Responsible for collect/ deposit/review of cGMP documents and arrangement for submitting the same to QA department after completion.
• Responsible to train the down line employee including workman for training in cGMP documents and revised documents.
• Responsible for proper arrangement and storage of material as per need.
• Responsible for any other activity from time to time which his supervisor/company feel appropriate.