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Do you want to join an international team within an innovative fast-paced medical device company? Grab the opportunity and make good use of your Mathematical and programming skills and affinity to medical device
Key Responsibilities:
You will deal with imaging, 3D modeling, surface reconstruction, image processing and high-performance computing.
You will understand the products and the customer needs.
You will research and analyze the underlying problems using real data.
Design and test algorithms in C++ and Python.
Implement algorithms in C++, and integrate them into the application.
Work closely with other members of the algorithms team and members of other groups such as physics and electronics
Participate in design reviews and code review of co-developers.

In this position, you will develop and execute regulatory strategy, work closely with R&D and Engineering departments to provide regulatory inputs relevant to product development and changes, write and submit submission packages to FDA, EU, and work closely with worldwide RA partners
Key Responsibilities:
In this role, you will
Actively contribute in the development of regulatory strategies for product development and approval, as well as product lifecycle maintenance. You will be able to support regulatory activities with different partners and their global strategy for product launch.
Perform coordination and preparation of document packages for US FDA regulatory submissions, EU MDD/MDR Technical Files, and international packages.
Coordinate and implement MDR requirements related efforts in the organization.
Assess product changes and their global regulatory impact.
Lead or compile all materials required in submissions, license renewal and annual registrations for internal and external partners.
Interact with internal marketing, R&D, QA, project managers as well as external Regulatory partners.
Recommend changes for labeling, design, manufacturing, marketing, and clinical protocols for regulatory compliance.
Perform and document regulatory assessments of life-cycle changes according to regulatory requirements of the U.S. FDA, E.U., and rest of world (ROW).
Identify and communicate regulatory risks and mitigations.
Respond to Information requests from regulatory Authorities.
Explore submission pathways and regulatory opportunities, and recommend the most appropriate route according to regulation and business needs and priorities.
Utilize strategic regulatory thinking along with technical expertise to implement regulatory strategies for post-approval changes.
Coordinate project submission timelines in multiple regions.

Senior Manager, our SAP, is an IT leadership position, reporting to our CIO, responsible for leading and mentoring a talented group of analysts, developers and testers to deliver business solutions on the current ECC and Future S4HANA SAP platforms. This is a customer-facing role that requires strong leadership skills, a sound technical foundation, a breadth of functional knowledge & the ability to work across multiple teams within IT, as well as business units to realize the goals of ERP-specific projects on our roadmap. It is a challenging position that requires excellent business and technical know-how as well as strong leadership skills.
Key Responsibilities
Drive the strategic roadmap for SAP.
Get influence and sponsorship for the strategic roadmap.
Lead a Global SAP group consisting of a talented team of system analysts, developers, and testers.
Attain a strong knowledge of industry business models and processes.
Deliver quality and scalable solutions that meet the needs of our digital transformation.
Manage resources, plan deliverables/milestones, and oversee the project deliverables with the goal of realizing our roadmap and release plan.
Research current trends, along with emerging technologies in related areas and provide insight and analysis on how they may positively or negatively impact the enterprise.
Work with project managers and IT lead to provide effort estimation towards future programs and projects.
Develop and maintain a governance model and safeguarding to enable releases and changes across multiple line of business.

Our IT- Production support team is seeking for NOC Engineer to work at our network operations center which is being established to monitor our scanners install base and services are serving a large number of dental companies worldwide, 24/7.

Reporting to the NOC manager, your role will include, but not limited to, monitoring, diagnosing, troubleshooting various production issues, and collaborating with our various team, ensuring business continuity and high service performance are kept.

The NOC Technician is also responsible for escalation and dispatching to other Tiers resources, functions and/or managers.

Key Responsibilities:
Ensuring our flows are working as planned.
Handling production incidents per our processes.
Developing and performing simple production handbooks to ensure business continuation.
Vulnerability management.
liaising with 3rd. party vendors, handling escalations to resolution.
Suggest/Develop new monitoring requirements.
Handover relevant shift reports.
Collaborating with global teams ensuring cross company flow health and incidents handling.
Responsible for maintaining the NOC process Up to-Date (KB articles etc.).

This position will be located in the Petah Tikva, Israel and will be responsible for providing financial support and leadership to our manufacturing operations group.
You will work closely with the global manufacturing teams to analyze business trends, provide financial guidance and be a key contributor to the achievement of operational objectives
Key Responsibilities
In this role, you will
Perform monthly closing activities including preparation and approval of journal entries, and inventory related account reconciliations.
Manage inventory and related transactions, including physical to perpetual to general ledger reconciliations, journal entries, audit explanations, and standard costs.
Analyze inventory adjustments over set thresholds and work with production control to determine root cause and corrective action.
Analyze operating costs including ad hoc studies incorporating plant staffing, capacity and utilization, Purchase Price Variance and Make/Buy analyses; as well as other cost related projects.
Manage the periodic requirements of manufacturing systems to ensure timing and accuracy of standards and gross margins and provide meaningful analysis of results.
Provide cost accounting support to cross functional areas as requested.
Direct the development and review of cost analysis reports and work with operations to formulate corrective actions.
Prepare and present reports and presentations to senior management.
Participation in the process of building the company's annual budget.
Interact with Internal Audit and the independent public accounting firm on quarterly reviews and/or annual audit including Sarbanes Oxley(SOX) matters.
Other duties may be assigned as needed.

We are looking for a HRBP Expert to join our team!
The HRBP role will support multiple global functions in iTero. We are looking for a strong candidate that will have a proven record of working effectively in a dynamic, fast-growing environment.
Key Responsibilities
In this role, you will
Work closely with the Extended of R&D staff members and other global functions, managers and employees.
Proactively support the delivery of global and local HR Processes.
Manage complex HR Projects cross-functionally and globally in a matrix organization.
Partner in recruitment for key talents for the internal client.
Design succession plan for key talents and key job positions.
Design and support OD and L&T activities for the internal client and as a member of the HR team.
Working closely with the local HRBP in the global.

As a Clinical Liason - field based, you will be the first point of contact for dentists in your region (Israel) and be responsible for clinical education, communication, and support of both external and internal customers. Your mission is to provide customers the best clinical education and help them to become expert on Invisalign technique, increasing their clinical confidence. You will be travelling around the designated area to visit doctors in their clinical practices to improve their knowledge about the Invisalign.
Key Responsibilities:
Drive growth and build clinical confidence of customers through education on our clinical protocols and ClinCheck software program as well as clinical troubleshooting
Provide medical expertise, training and guidance to marketing and commercial teams and ensure they have sufficient clinical knowledge and information regarding the company's products.
Investigate and Analyse Clinical-related customer inquiries, complaints, and adverse events.
Drive and accelerate clinical confidence for selected groups of doctors via specifically designed educational programs in close coordination with customer support and sales team.
Provide clinical support & education to orthodontists, dentists in private clinics as well as might do within DSO organizations and Universities
Develop peer-to-peer relationships with HCPs, teaching them treatment planning and new digital workflows within our ADP.
Work cross-functionally to execute & coordinate Align educational programs and supports the achievement of predefined business goals.
Contribute independently. May contribute through others on key projects
Work closely with the sales team to achieve business objectives for the assigned territory.
Independently Plan visits & group sessions independently and timely based on BRs with general supervision and alignment with the sales team. Recommends new approaches and seeks for opportunities to enhance HCPs learning curve and digital workflows adoption.
Conduct field visits independently at least 70% of the time.