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Job Details

Associate Software Validation Engineer

Company: PAREXEL
Location: Nottingham, England,United Kingdom
Reference: 49836BR
Closing Date: 22 Feb 19
Type: Not Specified
Salary (£): Competitive
Benefits:

Job Summary:

Following training, carry out work in accordance with relevant standard operating procedures and standardswhich may include but not limited to:Associate Engineer:· Execute detailed test specifications. Record and tracks detailed results.· Work closely with project team leaders throughout the entire software development life cycle.· Review all pertinent project documentation.· Respond to all inquiries regarding the project under test. ...

Requirements:

Following training, carry out work in accordance with relevant standard operating procedures and standards
which may include but not limited to:
Associate Engineer:


· Execute detailed test specifications. Record and tracks detailed results.
· Work closely with project team leaders throughout the entire software development life cycle.
· Review all pertinent project documentation.
· Respond to all inquiries regarding the project under test.
· Reports on Project testing status to Project team leaders.
· 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.
· Participate in formal performance review processesQualificationsUnderstanding of software testing techniques and test case development.

· Familiarity with database design and/or testing.
· Ability to handle multiple concurrent tasks.
· 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.Understanding of software testing techniques and test case development.

· Familiarity with database design and/or testing.
· Ability to handle multiple concurrent tasks.
· 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.

Apply for this job: Associate Software Validation Engineer

Contact Information:

Address:  PAREXEL International
The Quays
101-105 Oxford Road
Uxbridge
Middlesex
UB8 1LZ
England
Tel:  +44 1895 238000
Fax:  +44 1895 238494
Website:  Visit Our Web Site
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