Amneal Pharmaceuticals – Walk-Ins on 7th April’ 2024 for B.Pharm, M.Pharm, B.Sc, M.Sc Candidates


Amneal is a high-quality producer of solid and Injectable generic products and one of the fastest-growing global generics producers. We believe that the world is our family and we are committed for consistently producing high quality affordable medicines. Amneal is expanding its operations in India and invites people who share its value of relentless pursuit of quality, integrity, treating each other with respect and encouraging the very best in everyone to join the Amneal family.

  • Qualification: B.Pharm, M.Pharm, B.Sc, MS/M.Sc 
  • Experience : 02-06+years
  • Department: Quality Control OSD
  • Role: Officer/Senior Officer/Executive
  • Job Location: Ahmedabad, Gujarat
  • No. of Openings: 20

Venue Details:

  • Date: 7th April , 2024
  • Date: 9.00 AM – 12.00 PM
  • Venue: Amneal Pharmaceuticals Pvt. Ltd. Plot No 15,16,17 Pharmez, Sarkhej Bavla Highway, Vil. Matoda, Ahmedabad 382213
  • Contact – Chandani Daswani/ Jagdish Mathukiya ( 02714677700 )

Job description:

Walk-in Drive @ Amneal Pharma | 7-April-24 (Sunday) | Quality Control OSD

We are looking for competent, dynamic and motivated candidates for suitable positions for Quality Control unit for SEZ Matoda Plant, Ahmedabad.

Job Location: SEZ MATODA, Ahmedabad

Quality Control OSD

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 /equipments.
  • Have exposure for the preparation of calibration & Preventive maintenance schedule of laboratory instruments/ equipment’s.
  • 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 CAPA’s.
  • 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.

Note :

The candidate with good communication, inter personal skills, computer knowledge, exposure to cGMP/GLP, should have exposure of regulated plant.

Knowledge and understanding of regulatory requirements are essential (Preferred 21 CFR compliance).

You may walk in for the interview with your updated CV along with annual CTC proof, appointment letter, Increment letter, latest 3 months’ salary slips, Bank statement, Aadhar & PAN card and 2 passport size photographs.

Only Interested & Relevant candidates may share their updated profile with [email protected] & [email protected]

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