Quality control (analysit)Officer / Sr. Executive: HPLC / GC / IR / UV / Dissolution in Zydus pharmaceuticals
Pharmaceuticals jobs
Position: QC Analyst
Quality Control (Analyst):Officer / Sr. Executive: HPLC / GC / IR / UV / Dissolution and other QC Equipment/ QC Method Validation and Transfer.
Walk-In Interview Details Interview Date: 10th May 2026
- · Interview Time: 9:00 AM – 3:00 PM
- Interview venue: 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
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.