Beschreibung
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.