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

Description

• 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

• 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