Amneal Pharmaceuticals – Walk-In Interviews for Quality Control on 8th Aug’ 2021

Amneal Pharmaceuticals is an integrated specialty pharmaceutical company powered by a robust U.S. generics business and a growing branded business. Together, our team is working to build one of the most dynamic pharmaceutical companies in our rapidly changing industry.

Walk-in interview For QC OSD Rajoda and Matoda plant, A’bad. @ AMNEAL PHARMACEUTICALS PRIVATE LIMITED

We are looking for competent, dynamic and motivated candidates for suitable positions in Quality Control OSD (Oral Solid Dosage) unit for our Ahmedabad Rajoda & SEZ Matoda Plant.


  • All precautions pertaining to Covid 19 pandemic will be strictly followed.
  • Mask will be mandatory for all
  • Do not attend interview if suffering from any health issue (Cold, Cough, Fever or Sore Throat)

Date: 08th August, 2021 (Sunday)

Timing: 8:30 AM to 2:00 PM

  • Job Location : Rajoda & SEZ MATODA (OSD unit Ahmedabad)
  • Department : Quality Control
  • Designation: Officer/Senior Officer/Executive
  • Qualification: B.Pharm/M.Sc./B.Sc
  • Total Experience: 3 to 7 years

Desired Profile :

  • To perform analysis Finished Product, In-process and Stability samples as per respective STPs/SOPs/Specifications/protocols & Pharmacopoeial requirement as applicable
  • Have exposure on operation, calibration, Qualification and maintenance of laboratory instruments / equipment.
  • Have exposure for the preparation of calibration & Preventive maintenance schedule of laboratory instruments / equipments.
  • Should have knowledge for the preparation, handling & management of working/reference standards etc. as per requirements.
  • Should have knowledge for the SOP’s, STP’s and GTP’s preparation.
  • Should have QMS activities knowledge i.e. Change control, Deviations and CAPAs.
  • Have exposure for the preparation and standardization of volumetric solutions/reagents and to maintain related documents.
  • Specific exposure on XRPD, LCMS, GCMS, ICPMS, AAS, Method development, Method Validation
  • Knowledge to operate various analytical instruments – UV-VIS spectrometer, KF titration, dissolution test apparatus, Autotitrator, FTIR spectrometer, HPLC
  • Knowledge to perform all quality control activities with compliance to cGxP for instrumental, chemical and physical analysis

The candidate with good communication, inter personal skills, computer knowledge, exposure to cGMP/GLP Knowledge and understanding of regulatory requirements are essential (Preferred 21 CFR compliance)

Only Interested & Relevant candidates may share their updated profile with




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