PharmaTutor
19 March 2012

Job as Formulation Technologies Manager in Colorcon Asia

19 March 2012
Work as Deputy Production Manager in Bakson Drugs

19 March 2012
Work as (Associate) Scientific Liaison, Biologics and Biotechnology in US Pharmacopiea

The United States Pharmacopeia (USP) is a non–governmental, official public standards–setting authority for prescription and over–the–counter medicines and other healthcare products manufactured or sold in the United States. USP also sets widely recognized standards for food ingredients and dietary supplements. USP sets standards for the quality, purity, strength, and consistency of these products–critical to the public health.

19 March 2012
Government invites Pharmacist (Trainee) & Staff Nurses in South Eastern Coalfields - Freshers | Total 46 Posts

South Eastern Coalfields Limited invites applications from the willing candidates who fulfill required qualification for the following vacant posts. The details and other terms & condition are given below.After the appointment the candidates will have the benefit of other allowances, beside the Basic Salary, VDA, SDA as per rules of Coal India Limited under National Coal Wages Agreement-VIII.

18 March 2012
Job openings for Production Chemist, Packing Line Supervisor, QA-QC Chemist in Ultra Beauty Care

Ultra Beauty Care Pvt. Ltd., is a leading cosmetics manufacturing company based in Aurangabad (Maharashtra) with a state of the art manufacturing plant designed as per the Schedule M of GMP.
The company currently manufactures cosmetics on Loan License basis for leading brands. UBCPL is also involved in development of products to be offered to our exports clients on a regular basis in Europe & Africa.

18 March 2012
Require Fresh & Exp. B.Pharm and M.Sc, Ph.D, MBBS, MVSc as Scientists in B to H at NATIONAL INSTITUTE OF ANIMAL BIOTECHNOLOGY (NIAB), Government of India | Total 12 posts

18 March 2012
Work in J. Mitra Pharma | AM-HR, Trainee QA Officer, QA Executive, Research Associate, Manager Customer Service, ASM, Product Executive, Asst. Manager- QA

J.Mitra is mainly involved in the business of preserving Human life of critically unwell people. We aim At taking the utmost care of our clients as well as our employees. GROUP focus is on creativity, fresh ideas backed by empowerment, delegation and calculated risk taking. Our Endeavour is to create an environment where talent can reach to its peak & to do so we strive to make the workplace a source of creativity & innovation.

18 March 2012
STEM CELLS REGULATION

MOLECULES INVOLVED IN REGULATION OF STEM CELL DIFFERENTITIATION
Cell adeshive molecule E_cadhedrin which replaces oct 4signalling molecule there by converting normal somatic cell into pluripotent

18 March 2012
VALIDATED RP – HPLC METHOD FOR DETERMINATION OF MONTELUKAST SODIUM AND LEVOCETIRIZINE IN BULK AND ITS PHARMACEUTICAL FORMULATIONS USING UV-VIS DETECTOR

About Authors:
RAVISANKAR.M*1, SUBASINI.U2, ANAND THANGADHURAI.S3, KARTHIKEYAN.S4, CHANDRA SEKAR.E.5
1.Swamy Vivekanandha College of pharmacy, dept of pharmaceutical analysis. Thiruchengode
2.Swamy Vivekanandha College of pharmacy, dept of pharmacognosy. Thiruchengode
3.Swamy Vivekanandha College of pharmacy, dept of pharmaceutical analysis. Thiruchengode
4.Kausikh therapeutics and private limited.chennai
5.Swamy Vivekanandha College of pharmacy, dept of pharmaceutical analysis. Thiruchengode

ABSTRACT
An isocratic reverse phase high performance liquid chromatographic method for estimation of montelukast sodium and levocetirizine in bulk dosage and in marketed formulations has been devised and validated. The chromatographic separation achieved on shodex c18-4E column (5µm, 250 mm x 4.6 mm) and  acetonitrile: methanol: ammonium acetate buffer (PH- 5.5) in the ratio of 25:55:20 v/v. The flow rate was 1.0 ml/min and the UV detection was identified at 225nm.The retention times for montelukast sodium and levocetirizine was found to be 5.15 min and 3.12 min respectively. The linearity of montelukast sodium and levocetirizine is 10 -50µg/ml with the correlation co efficient 0.99 respectively. The validation parameters such as accuracy, precision, LOD, LOQ, Robustness, ruggedness were performed as per ICH guidelines. This method can be used for routine analysis of montelukast sodium and levocetirizine in bulk and marketed dosage forms.

16 March 2012
Walk in Interview for QC in Kemwell Pharma - 8 posts

Kemwell Pvt Ltd., established in the year 1972 at Bangalore, Specializes in contract manufacturing for pharmaceutical formulations for various reputed multinations in India. For its expansion plans is looking for yound dynamic personnel.

Post: QC - Executive

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