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Project Manager Software Development with Experience in the Medical Industry (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Support, Design
Projektbeschreibung
REFERENZNUMMER:
316244/4
IHRE AUFGABEN:
-Project management including planning and implementation of complex projects with several parallel work streams
-Drive actions among the cross functional team, in particular with software development, quality and regulatory functions, in a Medical Device/Combination product context
-Maintain project tasks, dates, calendars up to date using the defined PM tool set
-Author/route/manage workflows of regulated documentation as required in short timelines
-Draft, review and apply guidance (update) from other functions on design control documents such as essential requirement list, clinical evaluation report, plans, etc.
-Lead the preparation of the critical milestones meeting at the end of each of the development phases
-Prepare status updates for core team to provide visibility on status and upcoming problems to be solved
-Anticipate key upcoming Quality, Regulatory, Medical Safety, Privacy questions and work with relevant functions to get appropriate confirmations/guidance/support
IHRE QUALIFIKATIONEN:
-Experienced project manager with background in software development
-Experienced in GxP, regulated software development in the pharma industry and good documentation practices (preferably Digital Health)
-Able to operate independently as part of a geographically dispersed team
-Able to problem solve and be perseverant until an acceptable solution is found to support project timelines
-High level of responsiveness (Instant Messaging, mobile phone)
-Excellent communication/presentation skills as well as scientific/technical writing skills
-Fluency in the English language is required; any other language is a benefit
WEITERE QUALIFIKATIONEN:
Project manager
316244/4
IHRE AUFGABEN:
-Project management including planning and implementation of complex projects with several parallel work streams
-Drive actions among the cross functional team, in particular with software development, quality and regulatory functions, in a Medical Device/Combination product context
-Maintain project tasks, dates, calendars up to date using the defined PM tool set
-Author/route/manage workflows of regulated documentation as required in short timelines
-Draft, review and apply guidance (update) from other functions on design control documents such as essential requirement list, clinical evaluation report, plans, etc.
-Lead the preparation of the critical milestones meeting at the end of each of the development phases
-Prepare status updates for core team to provide visibility on status and upcoming problems to be solved
-Anticipate key upcoming Quality, Regulatory, Medical Safety, Privacy questions and work with relevant functions to get appropriate confirmations/guidance/support
IHRE QUALIFIKATIONEN:
-Experienced project manager with background in software development
-Experienced in GxP, regulated software development in the pharma industry and good documentation practices (preferably Digital Health)
-Able to operate independently as part of a geographically dispersed team
-Able to problem solve and be perseverant until an acceptable solution is found to support project timelines
-High level of responsiveness (Instant Messaging, mobile phone)
-Excellent communication/presentation skills as well as scientific/technical writing skills
-Fluency in the English language is required; any other language is a benefit
WEITERE QUALIFIKATIONEN:
Project manager
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Sonstiges