Beschreibung
Process Management Support (m/w) 100%Main / Project Tasks:
For our customer in the region of Lucerne we are looking for an Responsible for process management, process optimization, project interaction with the associated stakeholders/departments and documentation of various development projects (system and assay) in the areas of requirements management, product risk management, configuration management, verification and validation management and usability engineering
Main tasks:
- Conduct detailed product risk assessments by analyzing documents, statistics, reports and market trends and with a team of cross functional representatives
- Support translation of multi-level requirements via Requirements Management process
- Ensure implementation of Usability Engineering within the projects (requirements, risk traceability and guidance during execution of UE driven verification and/or validation activities)
- Establish and perform Configuration Management in complex development projects
- Support development projects as Verification Manager (Planning, Guiding, Training, Reporting)
- Contact person in case of questions with regard to Validation Management
Work / Professional Experience:
- Experience in Process Management (Product Risk-, Requirements-, Configuration- and/or Verification Management) is desired
- Experience in working with Databases
- Has preferably worked in the Diagnostics /Medical Device industry
- Is able to lead by influence, demonstrated effectiveness, drive decisions and account for results
- Can resolve conflicts and adapt to change, effective to drive results and achieve project goals
- Is a proficient communicator and presenter (in English, German is a plus)
- Is an open minded team-player
Education:
- Bachelor (or higher) degree in Life Sciences, Natural Sciences or Engineering
Sprachen:
- English - Proficient
Referenznr.: 918174KV
Role: Process Management Support (m/w) 100%
Branche: Pharma
Work location: Luzern und Region
Full-time: 100%
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