Technical Staff

Piramal Pharma

Madhya Pradesh, India6d ago

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Key details

Location
Madhya Pradesh, India
Work style
Onsite
Level
Senior
Job type
Full-time
Function
other
Focus area
other
Posted
6d ago

Skills

calibrationdata entrygmpsap

About the role

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Division

Piramal Pharma Solutions

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

Technical Staff

Job Description

Responsible for proper storage and dispensing of Raw and packing materials as per cGMP norms.
Responsible for data entry in S4 HANA (SAP) & eWMS system.
Well verse in handling and control of RM/PM/FG inventory
Responsible for compliance of regulatory requirements as per cGMP norms.
  • Responsible for timely and correct material dispensing and issuance to production for manufacturing.
  • Responsible for handling and storage of Raw materials.
  • Responsible for control of inventory of Raw materials.
  • Responsible for maintaining routine housekeeping in warehouse areas as per cGMP norms
  • Responsible for collect / deposit of cGMP documents and arrangement for submitting the same to QA department after completion..
  • Responsible for handling, maintenance, verification and calibration of equipment’s/instruments in warehouse.
  • Responsible for timely attend the trainings on cGMP documents and revised documents.
  • Responsible to ensure EHS (Environmental, Health and Safety) related activities to be completed on time and to support EHS activities as per the requirements.
  • Responsible for monitoring and maintenance of safety compliance at work place.

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