User Acceptance Testing (UAT) Coordinator

Basel  ‐ Vor Ort
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Beschreibung

Our client, one of the biggest pharmaceutical companies based in Basel, is looking for a User Acceptance Testing (UAT) Coordinator/Writer who has strong experience in UAT Scripting writing within a pharmaceutical environment.

This is a contracting role based in Basel and planned to start from July until the end of the year with extension opportunities.

Are you a User Acceptance Testing Coordinator/Writer with some understanding of Computer System Validation (CSV) and currently looking for your next challenge?

If so, please have a look at the opportunity we can offer you:

Tasks & Responsibilities:

  • Works with business UAT Lead, business departments and internal Informatics departments and teams to coordinate/or support the creation, execution and completion of UAT business activities required for system projects or MME activities
  • Lead or participate in UAT activities for one or multiple PDR systems
  • Ability to interpret and understand the system change requirements in the URS and other project documentation as required to facilitate UAT test criteria
  • Write user acceptance test scripts to ensure that all test criteria are met for any system upgrade/release and according to agreed timelines of the project and validation requirements are met
  • Additional activities can include coordination of testers during the UAT execution, training, troubleshooting and single point of contact for UAT activities
  • Good knowledge of ALM system to create and manage user acceptance test cases and for execution and tracking
  • Participates in other special projects, as and when assigned, or otherwise requested to support UAT activities
  • UAT Coordinators/Writers are expected to perform their responsibilities with increased independence
  • Consistently complies with all governing laws, regulations, Roche SOPs and other guidelines

Ideal Profile:

  • Bachelors Degree required (computer sciences, business or life sciences disciplines are preferred)
  • 5 years of relevant experience to system projects (in particular with UAT activities), at least some of which was gained in the pharmaceutical/biotechnology industry
  • Good previous experience of UAT script writing
  • Some understanding of CSV is preferred
  • Some understanding of international regulations, processes and issues in drug/biologics development
  • Fluent English

Please note, we can only consider EU/CH candidates or those with a valid work permit for Switzerland.

Are you interested with this opportunity and would like to have more information? Please get in touch with Florence Wespiser ( (see below) )

Start
ab sofort
Dauer
5 months with extensions opportunities
(Verlängerung möglich)
Von
Stamford Consultants AG
Eingestellt
30.06.2017
Projekt-ID:
1370743
Vertragsart
Freiberuflich
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