www.jaypar.com Software Pvt Ltd Bangalore : Sharepoint, MOSS, .Net Developer

[Admin]

Jaypar Software Pvt. Ltd Bengaluru/Bangalore : Sharepoint, MOSS, .Net

Designation: Sharepoint, MOSS, .Net
Experience: 4 - 8 Years
Location: Bengaluru/Bangalore

Job Description:
MOSS 2007, SharePoint Designer, WSS 3.0, Dot.Net
Installation, Configuration, Upgrade, Site Template Customization, Site Definition Customization, Content Management, Windows Workflow Foundation, Custom Web Parts, Reports, BDC ...

Desired Candidate Profile:
Microsoft Office SharePoint Server 2007 (MOSS 2007), SharePoint Designer, Windows SharePoint Services 3.0 (WSS 3.0)
Dot.Net: ASP.Net, C#, VB.Net, ADO.Net, Web Services
Database: SQL Server 2005
Knowledge of Sybase Power Designer required

Company Profile:
Jaypar Software is a global Information Technology consulting and services company committed to providing high-quality, on-time solutions to its clients. Jaypar offers services in Application Development, BI, and DW

Address:
301, Eden Park
Vital Mallya Road
Bangalore
Bangalore,Karnataka,INDIA 560027

Email Address: sunayanab@jaypar.com
Website: http://www.jaypar.com

Keywords: Sharepoint, Moss, .net, dotnet

[Guest-IJT]

Name : Ramesh Utlapally
Email : autlapally AT rediffmail.com
Designation / Skillset : Jr Manager
Subject : Application for the suitable position.
Dear Sir,
I am having about 7 years of Experience in that 5 Years in QC (Stability) 2 Years (AR&D) of experience in Formulation Analytical Research & Development (CPS - Formulation) and Quality Control. Presently working with Dr.Reddy's Laboratories Ltd. placed at Hyderabad.
Prior to this, I started my carrier as trainee and reached to the position of Officer in M/s. Aurobindo Pharma Limited, Later I worked for MNC M/s. Ranbaxy Laboratory Ltd,
While I am confident that my education and experiences have prepared me to give my level best services, I am excited about it where I expect my learning to increase exponentially into the future. I strongly believe that my positive attitude, excellent communication skills (including an ability to speak 3 languages fluently) will allow me to be a valuable asset to your organization.
I have enclosed my detailed resume for your review and consideration. I welcome an opportunity to discuss my experiences and qualifications with you in detail.
Thanking you,
Yours sincerely,
(Ramesh Utlapally)

Resume :
UTLAPALLY RAMESH,

Subject : Application for the suitable position.
Dear Sir,
I am having about 7 years of Experience in that 5 Years in QC (Stability) 2 Years (AR&D) of experience in Formulation Analytical Research & Development (CPS - Formulation) and Quality Control. Presently working with Dr.Reddy's Laboratories Ltd. placed at Hyderabad.
Prior to this, I started my carrier as trainee and reached to the position of Officer in M/s. Aurobindo Pharma Limited, Later I worked for MNC M/s. Ranbaxy Laboratory Ltd,
While I am confident that my education and experiences have prepared me to give my level best services, I am excited about it where I expect my learning to increase exponentially into the future. I strongly believe that my positive attitude, excellent communication skills (including an ability to speak 3 languages fluently) will allow me to be a valuable asset to your organization.
I have enclosed my detailed resume for your review and consideration. I welcome an opportunity to discuss my experiences and qualifications with you in detail.
Thanking you,
Yours sincerely,
(Ramesh Utlapally)
Objective :
To be the best in pharmaceutical industry, to be part of the team, contributing, acquiring knowledge and enhancing the skills both as professional and as a human being.

- Job profile in present position : (Nov 2007 to till date)
- I was done Registration Batches for analysis in other (Plant QC) department with team members.
- Investigate the Out of Trend (OOT), Out of Specification (OOS) and also investigate the Lab errors.
- Responsible for Method Validation and Stability studies for Drug Products as per the ICH Guidelines.
- Validation of analytical methods for Related Substances, Assay, Residual solvents Methods by using modern analytical techniques viz., HPLC, Dissolution and GC.
- Data generation & Technical document preparation : Like Method validation protocols, method validation data and stability compilation.
- Analytical method transfers within the group of companies and transfer of analytical methods to Quality Control Dept. after Method Validation.
- Actively participated in plant internal audits for compliance to USFDA and MCA audits.
- Lab compliance :
- Ensure that specifications and testing procedures are available in the laboratory.
- Designing preventive maintenance and calibration schedules for analytical instruments and ensure
the timely completion of the activities.
- Implementation smooth document flow and traceability within the departments.
- Assisted for adopting the control methodologies like change controls, OOS investigations, incidences associated with in the laboratory
- Review of preparation, in-house reference standards and working standards.
- Ensuring all the activities are carried out as per GLP, ICH and FDA guidelines norms laid in the department.
- Ensuring Lab safety.
- Maintain accountability for specific department activities in monthly reports.
Hierarchy : Reporting to Dept. Manager
- Job profile in M/s. Ranbaxy Laboratory Ltd (Nov’ 2005 to Oct’ 2007.)
- Analysis of Stability Samples for Region IV (US Market) ANDA filings and Preparation of analytical reports.
- Investigate the Out of Trend (OOT), Out of Specification (OOS) and also investigate the Lab errors.
- I have maintained dept and work planning, whenever my superior was absent.
- Analytical method transfers within the group of department and transfer of analytical methods to Quality Control Dept.
- Reviewing and compilation the data.
- Designing preventive maintenance and calibration schedules for analytical instruments and ensure
the timely completion of the activities.
- Lab compliance and documentation :
- As a team member completed laboratory set up right from Selection..
- Assisted for adopting the control methodologies like change controls, OOS investigations, incidences associated with in the laboratory.
- As a team member completed the equipment, installation & qualifications.
- Execution of periodic calibrations and maintenances.
- Preparation of In-house reference standards and working standards..
- Ensuring Lab safety.
Hierarchy : Reporting to Manager
- Job profile in M/s. Aurobindo Pharma Limited (Feb’ 2003 to Oct’ 2005)
- Analysis of Finished products (Related substances, Assay by HPLC and Residual solvents by GC)
- Qualification of working standards.
- Calibration of instruments, Like HPLC and GC
- Monitoring of finished and in process analysis and Review the raw data.
- Analysis of stability samples.
- Preparation of Documents to meet the cGMP requirements
- Actively participated in plant internal audits for authenticity, clear and accuracy of data for compliance to USFDA, MCA, ANVISA, and MCC audits.
Hierarchy : Reporting to Dept. Manager
- Training Programs Undergone
- HPLC method development, method validation and trouble shooting by Agilent technologies.
- On cGMP conducted by M/s Ascent consultants and trainers Pvt. Ltd. at Dr.Reddy's Laboratories Ltd.
- Technical Qualifications
- Postgraduate Diploma in Programming Concepts (PGDPC).
(MS Office, C-Language,)
- Technical Competencies
- Sound in analytical Method validations by using HPLC, Dissolution and GC for Drug Products and Drug Substances.
- Related substances and Assay by HPLC
- Related substances and Assay by GC
- Dissolution by HPLC, UV and GC (GC for Non-Chromophoric drugs).
- Residual solvents/Organic volatile impurities method by GC
- Operation and Calibration of the following Instruments :
- HPLC – Agilent, Waters, Shimadzu (HP-Chemstation, Chromeleon and Empower).
- Dissolution Apparatus-Electro Lab, Lab India.
- GC – Agilent, Shimadzu (HP-Chemstation, Chromeleon and Empower).
- KF & Auto titrator – Metrohm & Mettler.
- ADDITIONAL RESPONSIBILITIES :
- Documentation and review of Quality related documents.
- Trouble Shooting of Analytical Instruments and Methods.
- Validation and Qualification of Instruments as per regulatory requirements.
- Effective Time Management for completion of projects by planning with excellent Team co-ordination and support.
- Excellent strengths in Team management, oral and written communication skills.
- EDUCATIONAL QUALIFICATION :
- Master of Science (Chemistry) from Barkathulla Vishwavidylaya University.
- Bachelor of Science B. Sc-M.P.C) from Osmania University.

- References :
1. R Satyanarayana Murthy
Asst. Manager – AR&D
Dr Reddy’s Laboratory Ltd
Hyderabad.

2. M. VenuGopal
Manager-Satbility
Ranbaxy Laboratories Limited,
Paonta Sahib. (H.P)

(RAMESH UTLAPALLY)
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More Information about this submission and submitter :-
___________________________________________________
Submission ID : 4445871
Date & Time : 4th Aug 2011 5:00 PM (UTC)
IP Address : 202.65.144.164
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