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Zydus Lifesciences Ltd – Walk-In Drive on 20th Sep’ 2023

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
Time and Venue:
20th September, 9.30 AM – 5.30 PM
Zydus Lifesciences Limited (Formerly known as Cadila Healthcare Limited) Plot No. 265 to 267, Opp. Laxminarayan Petrol Pump, Sarkhej – Bavla, N.H. No. 8A, Changodar, Ahmedabad 382210

Job description:

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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