QC Analyst

Experience: 2 to 8 years

Location: Moraiya, Ahmedabad, India

Skills: HPLC, GC, IR, UV, Dissolution, SAP, LIMS, Current Valuable Laboratory Practices (cGLP), method validation, cleaning validation, stability protocols

Role name: QC Analyst Walk-In
Interview Details
· Interview Date: 10 th 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.

📌 QC Analyst (Ahmedabad)
🏢 Zydus Lifesciences
📍 Ahmedabad