Risk And Requirement Management Support

Luzern  ‐ Onsite
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Description

Reference #:5603NC

Industry: Pharmaceuticals

Location: Luzern und Region

Starting Date: ASAP

End Date: Till 30.06.2016

Workload: 100%

Accountabilities:
  • Gather, analyze, document and manage requirements within a project-wide shared database (HP ALM).
  • Ensure the database is up-to-date and accurate.
  • Ensure CRQ are translated into functional Product Requirements and lower level specifications.
  • Ensure traceability is complete and accurate.
  • Ensure requirement changes are agreed apon by all stakeholders and captured within the database with rationale and justifications.
  • Generate all requirements related documentation and deliver in time and in good quality.
  • Independently organize and lead meetings with cross functional stakeholders.
  • Ensure product risks arising from requirements changes, new requirements, primary operating functions, development studies, customer complaints, etc, are collected, recorded, maintained in the project-wide shared database for the life of the product.
  • Generate all risk related documentation and deliver in time and in good quality.
  • Escalate issues when things are not going according to plan
  • Independently run risk meetings with cross-functional stakeholders to gather feedback and agree on risk and ratings.


Responsibilities:
  • You are a motivated and quick learner
  • You are fluent in English (required); German a plus
  • Knowledge of PCR, medical devices is preferred
  • Bachelor of Science in Biology related field is preferred.
  • You are an active listener to be able to grasp and record minute
  • You have strong communication skills to facilitate meetings.
  • You are a detailed-oriented person, able to drill down from high-level information into details.
Start date
06/2015
Duration
Till 30/06/2015
From
ITech Consult AG
Published at
28.07.2015
Project ID:
954309
Contract type
Freelance
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