Software Engineering Associate, Production Synapse - RTSM

Recruiter
PAREXEL
Location
Nottinghamshire
Posted
11 Feb 2018
Closes
16 Feb 2018
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
.Associate Software Engineer• Rotational member in any of the RTSM Production teams at the direction of the Production Services Management Team.• Provide programming skills and expertise in the design and development of bespoke customer projects, change requests, reporting and technical support along with any production development activities.• Be responsible for the quality and timeliness of personally assigned workload to agreed timelines, standards and defined requirements. Bringing to the attention of management any circumstances requiring urgent or specific attention at the earliest opportunity.• Responsible for all of the unit testing of all code components produced.• Work closely with project team members throughout the entire software development life cycle.• Provision of technical advice to the internal and external study team, responding to technical queries in good time.• Participate in PMD process.• Delivering a positive, memorable and meaningful service which exceeds the expectations of both the internal and external customer.Qualifications.Job Qualifications:• Degree or higher degree in Computer Science, Engineering or related discipline,• Or equivalent work experience and have a demonstrable experience and interest in programming using any of the industry standard languages.Skills - Associate Software Engineer• 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.

Similar jobs

Similar jobs