Jodas Expoim Pvt Limited-  Walk-In Interview for AR&D Department on April 16th, 2023

Jodas Expoim Pvt Limited-  Walk-In Interview for AR&D Department on April 16th, 2023

Department: AR&D Department

Designation: Research Associate

Qualification: B.Pharmacy, M.Pharmacy, M.Sc

Experience: 2 to 8 years only

Job Description:

Analysis of Formulation Research Development samples. (Assay, Related Substances, Osmometer,

UV-Visible Spectrophotometer, Water Content).

Responsible for the analysis of the in process and Finished and Stability Samples.

Responsible for performing the analysis of HPLC, Assay and Related Substances by HPLC, Water Content by KF.

Responsible for online documentation of analysis done.

Responsible for online Support for Formulation department

Responsible for Good Laboratory Practices in Analytical Research and Development.

Responsible for Following the Calibration Schedule of the laboratory instruments as per master plan.
Operation & Calibration of Analytical Instruments (HPLC, Analytical micro balances & pH meter).

Candidates are requested to carry the last three months payslips, Recent increment letter. Original Certificates, Aadhar Card. Interested can send their resume to recruitments@jodasexpoim.in

Sunday 16th April 2023: (9.00 AM – 12.00 PM)

INTERVIEW LOCATION: JODAS EXPOIM PVT. LTD., 3rd Floor, NSL Centrum, Plot No S-1, Sy No: 1043 & 1048, KPHB Phase-III, Kukatpally, Hyderabad-500072, India.

WORK/LOCATION: JODAS EXPOIM PVT. LTD., BiotechPark, Phase III, Karkapatla

Job Category: pharma
Job Type: Full Time
Job Location: Phase III

Apply for this position

Allowed Type(s): .rtf

About Abha Maurya

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 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

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