Zydus Lifesciences Ltd – Walk-In Drive on 20th Sep’ 2023
The Zydus Group with an overarching purpose of empowering people with freedom to live healthier and more fulfilled lives, is an innovative, global lifesciences company that discovers, develops, manufactures, and markets a broad range of healthcare therapies. The group employs over 23000 people worldwide and is driven by its mission to unlock new possibilities in life-sciences through quality healthcare solutions that impact lives. The group aspires to become a global life-sciences company transforming lives through pathbreaking discoveries. The group has manufacturing sites and research facilities spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim in India and in the US and Brazil.
Zydus Lifesciences Walk In
- Qualification:B.Pharma ,B.Sc
- Experience: 02-03+years
- Role: Chemist
- Job Location: Ahmedabad
- Department: QA
- No. of Openings: 01
Issuance, archival, reconciliation, scanning and storage of documents as per SOP
Sampling and labelling of API/Saleable intermediate
To prepare, review master product label.
Packing of stability and Hold time sample & preparation/review of stability request/stability protocol in LIMS & withdrawal of stability samples
Reserve sample registration and annual verification of reserve sample and destruction of Reserve sample
Cleaning Sample collection as per ECR/cleaning protocol
To perform activities as per Site training coordinator role in ZyTIMS
To prepare, Review, Periodic Revision and implementation of SOP
To review executed documents (Batch manufacturing record/Equipment cleaning record/logbooks)
To perform Site oversite round, facility index, self-inspection.
To provide Line clearance in Manufacturing & physical verification of equipment during cleaning of manufacturing equipment.
To provide training to concern employees.
Perform vendor qualification related activities in SAP.
To prepare, Review, Periodic Revision and implementation of SOP.
To handle Trackwise module for QMS i.e. Change control, CAPA, Market complaint, Lab incident, OOS,OOT as per role defined.
To prepare/review trends/APQR
To approve Preventive maintenance of equipment and calibration of instruments in SAP.
Handling of Market sample / Reserve sample,.
To Prepare, review process validation protocol/report & Cleaning validation protocol /report
To perform dispatch activity,
To perform Bin verification and disposal of documents.
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