Risk- and Requirement-Management Support (m/f)

REFERENZNUMMER:

273483/11

IHRE AUFGABEN:

-Gather, analyse, document and manage requirements
-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 upon 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 during 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

IHRE QUALIFIKATIONEN:

-You are a detailed-oriented person, able to drill down from high-level information into details
-You are a motivated and quick learner
-You have strong communication skills to facilitate meetings
-You are fluent in English (required); German a plus
-You are an active listener to be able to grasp and record minutes
-Knowledge of PCR, medical devices is preferred
-Bachelor of Science in Biology or related field is preferred

WEITERE QUALIFIKATIONEN:

Quality manager