Change Control Manager - Rotkreuz, Schweiz - Workmanagement

Workmanagement
Workmanagement
Geprüftes Unternehmen
Rotkreuz, Schweiz

vor 1 Woche

Lena Schneider

Geschrieben von:

Lena Schneider

beBee Recruiter


Beschreibung
Are you looking for a new challenge? Then you've come to the right place


Thanks to over 40 years of experience in job placement, Workmanagement AG has secured an important position in various departments of well-known companies throughout Switzerland.

For our renowned client in the medical sector in Rotkreuz, we are looking for a


Change Control Manager (M/F/d):


Anstellung: 100%


Ort:
Rotkreuz


Branche:


Veröffentlichungsdatum:

Global Operations Consumables is the competence center for single-use injection molded parts in the diagnostic workflow.

This includes the development of new consumables, product care activities, the assurance of supply as well as the supplier selection and maintenance in close collaboration with Procurement.

It has expertise in all injection molding and plastic-relevant areas: Mold technology, polymers, automation, product design, supplier management, injection molding technique, plastics technology and material sciences.


Tasks & Responsibilities:


  • Managing change execution and change Coordination in the area of Global Operations Consumables with internal
stakeholders (e.g. - Quality Management) and external contract manufacturers

  • Responsible for the efficient implementation of changes within Roche and also at the the contract manufacturer
  • Responsible for maintenance and preparation of the regulatory correct documentation, for example Change Request/Change
  • Notification, Design Master Record, Design History File etc
  • Planning and implementation of work packages from product care projects with mínimal supervision
  • Being a proactive member of the squad
  • Identification of process improvements in the working area (e.g. change process)

Must Haves:


  • Work experience in change management or in project and process management
  • Practical experience in a regulated GxP environment, ideally in medical devices/IVD industry (ISO 13485, FDA 21 CFR 820, IVDR/MDR)
  • First professional experience in document management within a regulated environment
  • Good knowledge in SAP or comparable ERP system
  • Very good communication skills in German and English (spoken and written) are required Team player, independent and reliable way of working is expected.

What you can expect:


  • Challenging and varied work
  • Modern employment conditions
  • Longterm employment
I will be happy to provide you with further details.

Applications that do not meet the requirements cannot be answered/returned.

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