Company Name: PAREXEL International
Website: www.parexel.com
Package Offered : Best in Market
Location: Hyderabad
Experience Required: 0-2yrs
Educational Qualification: Degree or higher degree in Computer Science, Engineering or related discipline,Or equivalent work experience
Functional Area: Application Programming
Type of Industry: IT-Software Services
Required Candidate Skills :
Knowledge of working in a structured software development life cycle environment preferred but not essential.
Skills:
Knowledge of software development languages and tools such as C#, VB.net, Java and SQL.
Knowledge of Web/App Server environment i.e. Tomcat is preferable.
Knowledge of relational databases, preferably Oracle.
Familiarity with the software development lifecycle and testing methodologies.
Ability to prioritize work and meet deadlines.
Ability to work and communicate in a project team environment.
Ability to interpret and question project requirements documentation.
Ability to produce clear and concise technical documentation.
Some knowledge of clinical data management process for FDA regulated companies is a plus. Familiarity with FDA regulations such as 21 CFR Part 11 and GxP desirable.
CLICK HERE TO APPLY
Website: www.parexel.com
Package Offered : Best in Market
Location: Hyderabad
Experience Required: 0-2yrs
Educational Qualification: Degree or higher degree in Computer Science, Engineering or related discipline,Or equivalent work experience
Functional Area: Application Programming
Type of Industry: IT-Software Services
Required Candidate Skills :
Knowledge of working in a structured software development life cycle environment preferred but not essential.
Skills:
Knowledge of software development languages and tools such as C#, VB.net, Java and SQL.
Knowledge of Web/App Server environment i.e. Tomcat is preferable.
Knowledge of relational databases, preferably Oracle.
Familiarity with the software development lifecycle and testing methodologies.
Ability to prioritize work and meet deadlines.
Ability to work and communicate in a project team environment.
Ability to interpret and question project requirements documentation.
Ability to produce clear and concise technical documentation.
Some knowledge of clinical data management process for FDA regulated companies is a plus. Familiarity with FDA regulations such as 21 CFR Part 11 and GxP desirable.
CLICK HERE TO APPLY
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