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Piramal Pharma SolutionsPiramal 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 StaffJob Description
Responsible for Dispensing and issuance of Raw Materials 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 to coordinate with cross-functional department, Production, QA, QC, Engg, planning for smooth planning and follow-up as per routine activities in warehouse.
Timely dispensed and issuance of batch as per manufacturing requirement and arrangement of in process container (IPC) and planning for timely batch releases.
Responsible for pre-dispensing activities, Assay/potency calculation in BMR, material retrieval, preparation of material provision and printing of dispensing label from SAP, (If SAP user ID is available).
Responsible for correct data entry and handling of WMS program in SAP system, (If SAP user ID is available).
Responsible for control of inventory of Raw materials.
Responsible for maintaining routine housekeeping in warehouse areas as per cGMP norms. Responsible for disposal of rejected/LRN and Write-off materials and its documentation. Responsible for coordinate with Planning/Purchase/QC/Production for minimize inventory of Raw, Packing and Engineering materials to avoid slow moving/non-moving and near expiry inventory.
Responsible for collect / deposit of cGMP documents and arrangement for submitting the same to QA department after completion.
Responsible for any other activity from time to time which his supervisor/company feel appropriate.
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.
To report near miss and incidences as observed as per EHS requirement.
Support to site DICO (Data Integrity Compliance Officer) for monitoring and implementation of actions related to Data integrity awareness at site.
To ensure data integrity compliances at site and while performing activities.
Responsible for monitoring and maintenance of safety compliance at work place.
Responsible to maintain good hygiene, safety practices and cGMP practices.
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