www.avmhospital.com AVM Hospital Tuticorin : Physician, Resident Medical Officer

[Admin]

avmhospital.com

A 200 bedded Multi Speciality Hospital requires Medical Professionals for the following positions :

1. Physician - 2 Nos.
Qualification : M.D
Experience : Minimum 5-10 years
Age limit : 45 yrs

2. Resident Medical Officers - 7 Nos.
Qualification : MBBS
Renumeration as required.

Accommodation shall be arranged.
Both Male and female can apply.


Mobile : 9443125169

AVM Hospital

135 Palayamkottai Road, TUTICORIN 628003, TAMIL NADU


AVM hospital Established in the year 1992 is situated in an area of 1 acre and 31 cents and is a multi-storeyed structure. The hospital has total bed strength of 120 in three floors and has every type of accommodations.

http://www.avmhospital.com

[Guest-IJT]

Covering Letter

Respected,
Sir/Madam
I am Deepak sen, working with “USV Limited” for the more then past Three years , which is a Mumbai, based Biotech Company. Presently I am working on ANDA Biotech project in Biotech research laboratory in analytical section. which includes Synthetic peptide and recombinant protein, with modern techniques of analytical method development, validation and technology transfer for in process, final API and formulation The wide exposure that I have on various aspects like Recombinant protein down stream process, with different method development like SEC, RPHPLC, IC and many more type of HPLC work on Biology that gives me confidence that I will be able to grasp and do job / Research on new topics. My total experience is 7 years in Analytical pharma and biotech. From last four years I am with biotech research. I would like to draw your kind attention for the perusal of my C.V and to consider my application for the position. I will be privileged if I get an opportunity to work with you.

Thanking you for your valuable time and consideration.

Yours Sincerely,
Deepak sen.

DEEPAK SEN
M.Sc [Chemistry]
Sr Research Associate – Biotechnology research Laboratory
USV. LTD
Email : dsen_79 AT yahoo.co.in

Profile :
I would describe myself as highly motivated, creative, initiative, organized individual, who would thrive on challenges and has the ability to adopt with situation of stress and relate well with the people. I would like to seek a challenging position with a dynamic group with excellent growth opportunities in the field of Analytical Research & Development. I Have a Very good Experience in Audit Of MHRA, FDA, US-FDA, and internal Audit also.

Professional Summary :
Having experience of 7 years in Pharma and biotechnology industry in fields of Bio-tech research laboratories and Analytical Research and method development and validation with thorough knowledge of validation of Analytical method, & related documents for cGMP & GLP conditions.

Current Industrial Experience :
Working as an SR. Research Associate in Bio-tech research laboratories for Synthetic peptide and recombinant protein, in USV. LIMITED. Joined on September 2007.


Experience : 1
- IPCA LABORATORIES LTD. ATHAL – (SILVASSA)
- Designation : - Jr.Officer
- Duration : Feb 2002 to Oct 2004
- Department : Quality Control


Experience : 2

- MJ BIOPHARMA LTD
- Designation : - Sr.Officer (AMD)
- Duration : Nov 2004 Oct 2007
- Department : - Analytical Method Development

Current Job Responsibilities :
Working for ANDA Biotech product for development of Assay analytical method and related product with other necessary method with validation part.
Job Responsibilities in Bio-tech research laboratories and analytical method development of ANDA analytical method for Recombinant protein.
- Involved in Protein Analytical Method Developmental Stage to submission of Trial batches i.e. Test Methods development and standardization, Documentation, submission of experimental batches.
- Preparation of Analytical method Validation Protocol and Conducting Method validations as per ICH Guidelines
- Preparation of Reference and Working Standard for Different type of analysis requirement.
- Preparation of Product release Specifications, COA’s and Test methods for Recombinant Protein.
- Preparation of protocol and conduction of Stability Studies (Real time, Accelerated), as per ICH Guidelines on Final bulk and final Product.
- Preparation and review of documents like SOPs, validation protocols, Equipment URS and other related documents.
- Planning for Analytical method transfer.
- Regular Analysis of the Intermediate products- for Protein.
- Procurement and installation of equipments required for Bio-tech research laboratories Lab
- Preparation of Monthly and Quarterly reports
- Training to colleagues on testing.


Job Responsibilities in Process and analytical method development of Synthetic peptide
- Preparation of working standard for different analysis.
- Development of Analytical Assay for Synthetic peptide.
- Technology transfer for Intermediate and final API with supporting method and document like tech –transfer document. Along with product information.
- Provide to complete analytical support to Synthetic peptide department with in process sample analysis.
- Preparation of R&D Sop’s, validation protocols and other related Documents.

Training Programs Attended :
- Attending a monthly safety and cGLP training program.
Additional Information :
I had completed also Diploma in pharmacy with Diploma in computer programming and application. And I am interest to involve in Biological discussion.

Computer Skills :
MS – WORD, MS – OFFICE, OPEN Office.
Education :
Course : B.Sc. Chemistry.
Year of Passing : 2005
University : BKD University, Jhansi.
Course : Diploma in pharmacy
Year of Passing : 2002
University : Bangalore University, Karnataka.
Course : M.Sc. Chemistry
Year of Passing : 2009
University : MKU University,

[Unregistered]

Respected sir,
If there any nursing college will be started. I finished bsc nursing. So only I ask sir. Can I know that sir.
Thanking you