Neuland Laboratories Limited – Walk-In Interviews on 28th – 30th Nov’ 2019 @ Hyderabad
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Walk – in Interviews for Wet, GC & HPLC Candidates
Date: 28th – 30th November, 12 PM onwards
Neuland Laboratories Ltd,
Unit – 2, Plot Nos : 92,93,94,257,258,259,
IDA, Pashamylaram, Isnapur, Patancheru Mandal,
Medak District, 502319, Telangana, India
Contact – N Sushma (08455302187)
- Responsible for sampling as per SOP and perform the analysis.
- Analyses the samples as per specification and method of analysis and reports the results in analytical reports.
- Calibrates the Instruments/Equipments in Q. C. Department
- Carryout analysis of Finished samples, Commercial samples and Recovered solvents sampling and testing.
- Carry out analysis by KF auto titrator, Auto titrator, IR, PSD, SOR and UV spectrophotometer.
- Testing of various intermediates & finished products as per the current specification and methods of analysis.
GC & HPLC:
- Testing of various Raw materials, Intermediates, Finished products and Vendor samples as per the current methods of analysis by HPLC.
- Documentation of relevant calculations pertaining to the analysis
- Responsible for filling the complete analysis format of above without leaving any blanks and review the documents.
- Instrumentation analysis related to method of validation, stability samples and cleaning samples as per the respective specification, method of analysis and protocols
- Carryout Instruments/Equipment’s Calibration like HPLC, Balance, pH meter etc.,
- Maintenance of HPLC column.
- Reconciliation of impurities of respective products.
- Reviewing and carrying checked by for analytical worksheets and relevant data’s.
Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field.
During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube