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
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)