PHARMA WISDOM

PHARMA WISDOM

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Wednesday 22 March 2017

AUSHADH-2K17: One Day National Conference on "Pharmacoeconomic Shift & Quality of Life" on 25th March, 2017 @ VIPER

13:57:00 0
Greetings from "Vishnu Institute of Pharmaceutical Educational and Research". 
Now VIPER is going to organize its “AUSHADH 2K17" which is scheduled on 25th March, 2017 at college premises.  The theme of the conference is “Pharmacoeconomic shift and Quality of life”. The conference has planned an exciting scientific program that intends to share experiences with the delegates, the advances that are currently emerging globally in the economics in relation to quality of life. The scientific program includes Key note address by eminent speakers, plenary lectures, scientific poster and oral (podium) presentations. VIPER intends to invite leaders from pharmaceutical industry, academia and regulators to explore the change that is required for the new breed of pharmacists. We are aware of your contribution in this area and particularly your familiarity with the developments that are currently happening in the Pharmacy Profession in India. 
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Tuesday 21 March 2017

Multiple Job Openings for Chemists / Assistants / Executives / Asst. Managers in Production / QC / QA / R&D / AR&D / RA / Maintenance Dept. @ SHODHANA LABORATORIES LTD

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Monday 20 March 2017

Pharm.D - IInd Year UNIVERSITY EXAMINATION PREVIOUS QUESTION PAPERS (2012 to 2016) - JNTU HYDERABAD

23:25:00 6

Pharm.D-SECOND YEAR EXAMINATION PREVIOUS QUESTION PAPERS JNTU HYDERABAD

PHARM.D II YEAR QUESTION PAPER - 2012
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PHARM.D II YEAR QUESTION PAPER - 2013
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PHARM.D II YEAR QUESTION PAPER - 2014
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PHARM.D II YEAR QUESTION PAPER - 2015
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PHARM.D II YEAR QUESTION PAPER - 2016
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Urgent Openings for Freshers as Drug Regulatory Trainee @ AILEX Pharmaceuticals Pvt. Ltd

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Multiple Vacancies in Quality Department @ Torrent Research Center

08:04:00 0
Dear Candidate,
Greetings from Torrent Research Center
This is to inform that we have Multiple Vacancies for Quality Dept.
Designation: Scientist-II
Department: Quality (RA)
Please find the Job Description given below:
-        -  To review PDR, MFC, IPS, specification and STPs of KSM, RM, intermediates and final API
-         - To review the technology, transfer documents like STPs, method validation protocol and report, characterization data, raw material specification, packaging material specification, finished product specification, stability. protocol and MPDs
-         - To review the manufacturing documents like MFC, BMR, BPR, process validation protocol/report, stability protocol/report, sampling protocol, process validation protocol and product development report
-         - To review and evaluate documents facilitates its usage for commercial purpose of API/KSM/Intermediates.
-         - To review outsourced DMF review for all market such as US, EU, Brazil, ROW etc.
-         - To compile amendments, annual reports, DMF / CEP as per the regulatory guidelines and take care of DMF extension
-        -  To evaluate the queries raised by Regulatory Authority and prepare draft response
-         - To initiate and assess change control and validation form
-         - To evaluate API G1 report, brazil regularization, eCTD publishing
-         - To evaluate change notification/its impact for all market
-         - To communicate with vendor for API related issue
Interested candidates are requested to send their updated CV on this mail Id
mihiradhvaryu@torrentpharma.com
With Regards,
Mihir Adhvaryu
Human Resources
Phone: +91-79-239 69100 EXT: 138
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