Beschreibung
Process Manager Support @ Roche Diagnostics 100%Background:
Process and Support is part of the Global Roche Molecular Diagnostics (RMD) Development organization with two teams which are located in Pleasanton, USA, and Rotkreuz, CH. Both teams are focused on supporting and managing the processes and procedures for RMD Development, with multiple core competencies, functions, tasks and interactions.
The Process Management Team provides support to the RMD Development Teams (Assay, Software, Instrument, and System Development) regarding Requirements and Risk Management, Configuration Management, Verification and Validation Management, and Usability Engineering. This requires close interaction with several internal functions in order to gather all necessary information needed to ensure high quality documentation.
Role:
In this role your main responsibilities will consist of (but will not be limited to):
* Responsible for process guidance, process optimization and documentation of various development projects (system and assay) regarding Requirements- and Risk-Management, Configuration Management, Verification and Validation Management, and/or Usability Engineering
* Support translation of multi-level requirements via Requirements Management process
* Conduct detailed risk assessments by analyzing documents, statistics, reports and market trends and with a team of cross functional representatives
* Ensure all risks and requirements are maintained within a database and streamline approach across projects
* Ensure the delivery of timely and good quality documentation
* Establish and perform Configuration Management in complex development projects
* Support development projects as Verification Manager (Planning, Guiding, Training, Reporting)
* Managing project related interactions with Development, Global Platform Support, Design Quality Assurance, Regulatory, Medical Affairs, external suppliers and other internal departments
* Information gathering from respective stakeholders including consolidation of information
* Independent execution of work packages within area of responsibility
* Organize and manage their own time within scope of assigned work packages
* Ensure the delivery of timely and good quality documentation
Requirements:
* At least University degree in Life Sciences, Natural Sciences or Engineering or similar (university leavers should send an application letter) or an education with minimum one year process management experience (technical education is an advantage)
* English fluent in written and spoken and German B1 level (good)
* Excellent communication and presentation skills
* Good Knowledge in documentation
* Good analytical thinking, a structured, reliable working manner, ability to prioritize, plan and manage multiple tasks and to instill a sense of urgency in teams
Nice to Have:
* Experience in the Diagnostics industry desired
* Ability to lead by influence, demonstrated effectiveness, drive decisions and account for results; ability to resolve conflicts and adapt to change, effective to drive results and achieve project goals
* Teamplayer
* Database experience preferred
Reference: 918916
Industry: Medical Devices
Location: Region Zug
Start: ASAP
Duration: 12 Months +
Work Load: 100%
About us:
ITech Consult is a certified ISO 9001:2015 Swiss company with offices also located in Germany and Ireland. ITech Consult is specialised in delivering IT candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.
Contact me for further information regarding our company, our positions or our attractive payroll-only-program: .