Job Position : Software Engineer - Enterprise JAVA
Job Designation : Software Developer
Job Category : IT / Software
Compensation : INR 3,50,000 - 5,00,000 P.A
Desired Education : BE/B.Tech (Computers) / MCA / M.Sc
Desired Experience : 0 to 2 Years
Key Skills : Core JAVA, JSP, Spring, OOAD, Jquery, HTML5, BootStrap,
Hibernate4
about company:
PAREXEL IS
Service revenue from the PCMS business segment represented $167.1 million, or 12.0%, of consolidated service revenue in
Fiscal Year 2012, $129.7 million, or 10.7%, of consolidated service revenue in Fiscal Year 2011, and $121.7 million, or 10.8%,
of consolidated service revenue in Fiscal Year 2010.
We conduct our PCMS operations through five groups:
• Integrated Product Development Consulting – Our Integrated Product Development (“IPD”) consulting group
provides comprehensive product development and regulatory consulting services for pharmaceutical, biotechnology,
and medical device companies in major jurisdictions in the U.S., Europe, Japan and emerging markets in Asia, Middle
East and North Africa, and Latin America. These services include drug and device development and regulatory
strategy design, scientific and technical evaluation, writing and review services, preparation, review and submission of
regulatory applications (both for clinical trials and for marketing authorizations) to regulatory authorities in dozens of
5
countries, regulatory training for client personnel, and expert liaison with the FDA, EMA, and other regulatory
agencies around the world. Our IPD consulting group works closely with clients to design product development and
regulatory strategies and comprehensive registration programs. Our product development and regulatory experts
include individuals who have joined us from the biopharmaceutical industry and regulatory agencies such as the FDA
and agencies in the U.K., Germany, The Netherlands, Sweden, and France. Our experts review existing published
literature and regulatory precedents, evaluate the scientific and technical data of a product (Non-Clinical, Clinical,
CMC, Regulatory) based on their individual and collective expertise and experience, assess the competitive and
regulatory environments in specific relation to our clients’ products and business goals, identify deficiencies in client
product documentation (“gap analysis”), and define the steps necessary to obtain regulatory approvals in the most
expeditious manner. Through these services, we help our clients obtain regulatory approval for particular products or
product lines in markets around the world.
Candidate Profile :
# Ability to write simple to complex DB queries, good understanding of database table
structures and constraints and also ability to do simple DB designing.
To write simple stored procedures Time-management, ability to prioritize the tasks.
Job Description :
# Ability to understand the OOAD design and develop Java code required to meet
requirements.
# Hands on experience on Core Java, Spring 3 and Hibernate4 Front end Technologies - JSP,
HTML5, JQuery, BootStrap
# Standard coding practices is must
CLICK HERE TO APPLY
Job Designation : Software Developer
Job Category : IT / Software
Compensation : INR 3,50,000 - 5,00,000 P.A
Desired Education : BE/B.Tech (Computers) / MCA / M.Sc
Desired Experience : 0 to 2 Years
Key Skills : Core JAVA, JSP, Spring, OOAD, Jquery, HTML5, BootStrap,
Hibernate4
about company:
PAREXEL IS
Service revenue from the PCMS business segment represented $167.1 million, or 12.0%, of consolidated service revenue in
Fiscal Year 2012, $129.7 million, or 10.7%, of consolidated service revenue in Fiscal Year 2011, and $121.7 million, or 10.8%,
of consolidated service revenue in Fiscal Year 2010.
We conduct our PCMS operations through five groups:
• Integrated Product Development Consulting – Our Integrated Product Development (“IPD”) consulting group
provides comprehensive product development and regulatory consulting services for pharmaceutical, biotechnology,
and medical device companies in major jurisdictions in the U.S., Europe, Japan and emerging markets in Asia, Middle
East and North Africa, and Latin America. These services include drug and device development and regulatory
strategy design, scientific and technical evaluation, writing and review services, preparation, review and submission of
regulatory applications (both for clinical trials and for marketing authorizations) to regulatory authorities in dozens of
5
countries, regulatory training for client personnel, and expert liaison with the FDA, EMA, and other regulatory
agencies around the world. Our IPD consulting group works closely with clients to design product development and
regulatory strategies and comprehensive registration programs. Our product development and regulatory experts
include individuals who have joined us from the biopharmaceutical industry and regulatory agencies such as the FDA
and agencies in the U.K., Germany, The Netherlands, Sweden, and France. Our experts review existing published
literature and regulatory precedents, evaluate the scientific and technical data of a product (Non-Clinical, Clinical,
CMC, Regulatory) based on their individual and collective expertise and experience, assess the competitive and
regulatory environments in specific relation to our clients’ products and business goals, identify deficiencies in client
product documentation (“gap analysis”), and define the steps necessary to obtain regulatory approvals in the most
expeditious manner. Through these services, we help our clients obtain regulatory approval for particular products or
product lines in markets around the world.
Candidate Profile :
# Ability to write simple to complex DB queries, good understanding of database table
structures and constraints and also ability to do simple DB designing.
To write simple stored procedures Time-management, ability to prioritize the tasks.
Job Description :
# Ability to understand the OOAD design and develop Java code required to meet
requirements.
# Hands on experience on Core Java, Spring 3 and Hibernate4 Front end Technologies - JSP,
HTML5, JQuery, BootStrap
# Standard coding practices is must
CLICK HERE TO APPLY
