לוח משרות דרושים בטירת כרמל

What you will be doing
Production Planning, develop, monitor and update detailed production plans to ensure timely completion of production schedules. Coordinate with production team to align resources and timeline. Material Coordination, ensure material availability for production by coordinating with procurement and warehouse teams. Report material shortages for the short -term production, track and follow up. Subcontractor Management, build and manage detailed production plans including forecast for subcontractor, ensuring alignment with overall production schedules. Capacity Planning, evaluate production capacity and recommend adjustments to meet short-term and long-term goals. Identify bottlenecks and implement solutions to enhance efficiency. Engineering Change Orders (ECO), implement and execute the material related aspect for ECOs in the production workflow and inventory. Inventory Management, Implement and maintain inventory methodology principles for efficient material usage.
* Working according to our Quality Policy, relevant Quality Procedures & Standards, and privacy & safety rules.

What you will be doing:
* You will be taking part of developing the heart of the SW in our products.
* You will experience in software development Python & C / C ++.
* Examine full development of project including DevOps processes.
* Be part of developing for a top medical company with high impact on people day life.
* Experience in working with hardware/ Embedded systems (eg. Raspberry pi, Arduino).
* Communicative, self-motivated, and self-learning.
* Working according to our Quality Policy, relevant Quality Procedures & Standards, and privacy & safety rules.
* Work in an Agile environment.
 
Advantages:
* Experience in Medical Device industry.

What you will be doing:
* Provide regulatory support to the Development and Post marketing activities related to our products.
* Preparation and maintenance of regulatory submissions and registrations of our products in relevant markets.
* Review complex reports, validations, etc. for scientific merit and regulatory appropriateness; Provide technical review of data or reports that will be incorporated into regulatory submissions to assure scientific rigor, accuracy, and clarity of presentation
* Preparation and maintenance of annual renewals of Establishment Registrations, Device Listing, and other pertinent regulatory licenses.
* Review of customer complaints to determine reportability according to regulatory requirements and execution of reporting per determination.
* Provide ongoing regulatory support and assessments to different QMS related processes (e.g. MRB, CAPA, Contract review)
* Actively participate in the evaluation of changes to the QMS documents and device design/process for impact on pending or existing registrations
* Provide support for all external/internal audits at HQ and globally, as needed
* Advise project teams on premarket regulatory requirements, labeling requirements and/or other compliance issues.
* Work closely with various other teams (e.g. R&D, Operations, Quality, Marketing) both locally and around the world, to provide regulatory inputs as needed.
* Monitor and advise the organization of upcoming or new guidance, regulations, agency/industry initiatives, etc. to ensure ongoing regulatory compliance
* Attend other regulatory related needs, as required
* Working according to our Quality Policy, relevant Quality Procedures & Standards, and privacy & safety rules.