Zydus Lifesciences Walk-In 10th May 2026 B.Sc / M.Sc / B.Pharma / M.Pharma for Multiple Positions

Zydus Lifesciences Walk-In Interview Details

  • Interview Date: 10th May 2026
  • Interview Timings: 9:00 AM – 3:00 PM
  • Interview Location: Zydus Healthcare Ltd, Block 2, 3, 4, 5, Sigma Commerce Zone, Nr. Iskon Mandir BRTS Bus Stand, Ambli Bopal Road, Ahmedabad – 380015.
  • Job Location: Moraiya, Ahmedabad
  • Education Qualification: B.Sc / M.Sc / B.Pharma / M.Pharma
  • Experience: 2 – 8 Years

Quality Control (Analyst):

  • Ø  Officer / Sr. Executive: HPLC / GC / IR / UV / Dissolution and other QC Equipment/ QC Method Validation and Transfer.

Job Responsibilities:

  • To perform the sampling of raw material and re-test material.
  • To perform Analysis of raw material/packaging material/in-process samples/intermediate/bulk & finished products/ process validation samples/ stability samples/ cleaning validation/method transfer sample etc.
  • Ensure/check proper cleaning of QC glass wares/tools/apparatus.
  • To make entries in SAP and LIMS as per requirement.
  • To maintain the equipment/instrument in operational, calibrated and qualified condition.
  • To handle, store the testing samples as per the respective material/ product requirement.
  • To charge Stability samples as defined in SOP and stability protocols.
  • To handle and dispose the testing samples/rejections after completion of analysis as per SOP.
  • To ensure all primary standards/working standards/certified standards/reference standards are stored as per the storage conditions specified and documented.
  • To ensure laboratory inventory management.
  • To initiate incidence/ OOS/ OOT/ OOC/ Deviation /CAPA /Change control and investigate (if required) under consultation with the department head/section head.
  • To prepare the specification, standard operating procedure, general test procedure and any other applicable document for quality control department.
  • Responsible for maintaining a neat and systematic work area at all times.
  • Responsible for following Current Good Laboratory Practices (cGLP).
  • Identify and report quality issues.
  • Report accidents and unsafe conditions or unusual circumstances to section in-charge/ head.
  • Other duties, which may be assigned from time to time, by reporting manager.

Essential job requirements:

  • Understands the purpose and function of analytical process and equipment/instrument.
  • Execute procedures for analysis in accordance with standard test procedures (STP), general test procedure (GTP), protocol and related SOPs.
  • Ability to document in logbooks, Test data sheets while performing the job using good documentation practices.
  • Attention to detail and ability to write and record data as per ALCOA policy.
  • Comply with the Privilege rights matrix (PRM) of the Organization.

SWARNALATHA B

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