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We are seeking a highly motivated, detail-oriented team player to join the CEO Office as a Strategy & Corporate Affairs Project Manager.

The Strategy & Corporate Affairs Project Manager will report to the VP, Strategy & Corporate Affairs & Chief of Staff, partnering closely with senior leaders to execute key projects, deliver business insights, and strengthen organizational alignment.

This role will support and drive cross-functional strategic initiatives and projects that shape the companys direction.

The ideal candidate is passionate about working with data and AI tools - someone who not only spots patterns but also tells the story behind the numbers, translating insights into strategic actions that drive business growth.

Key responsibilities:
Drive cross-functional strategic projects, ensuring milestones, timelines, and deliverables are met.
Prepare presentations, reports, and materials for senior leadership and board meetings.
Support the CEO Office and strategic agenda by managing priorities, following up on action items, and preparing for meetings.
Track project progress, identify issues, and recommend solutions to keep initiatives on track.
Provide business insights by analyzing data to identify trends and deliver clear, actionable recommendations to business leaders.
Monitor KPIs to track progress, surface risks, and support business goals
Help define and update KPIs to align teams around key objectives
Research data sources to support planning and analysis.
Test and apply new tools and technologies, including AI, to enhance reporting and project execution.
Collaborate with senior leaders to execute key projects and drive business growth.

Manages and train Regulatory Affairs representatives and associated processes for preparation of product submissions, including 510(K), CE Technical Files (MDD and MDR), China, Canada, Japan, South Korea, and Australia and other International Countries.
Interact with Internal and External teams on regulatory related projects to meet regulatory compliance topics and regulatory tasks.
Lead the development and implementation of regulatory strategy for assigned projects of the relevant BU
Collaborate with Sr. Director Regulatory regarding EU, China, Japan, South Korea, Taiwan and other global territories regulatory teams for to implementation of develop global regulatory strategies for projects and submissions.
Approving labeling (including advertising and promotional materials) in the context of submissions or registrations and serving as the regulatory expert of the projects.
Provide regulatory advice and guidance to Regulatory Affairs representatives, engineering, and project teams to ensure submissions meet regulatory requirements and maintain up-to-date knowledge of regulatory requirements.
Manage, mentoring and train International Regulatory Associates/Leads for product submissions.
Will support and partner with Internal teams and functions in phases of design, development, production, and distribution of medical devices.
Monitor emerging trends regarding industry regulations to determine potential impacts on organizational processes.

We are looking for a Product Manager for the Aesthetics Business, which includes a broad portfolio of leading solutions in the market as well as an exciting innovation pipeline. The Product Marketing Manager will be responsible for driving the business growth of the assigned product portfolio and oversee the 360 product marketing aspects of the products.

We are based in Yokneam, Israel (with offices also in Tel-Aviv).

Key responsibilities:

Owns and leads all product aspects relating to the assigned products, from product inception to launch and throughout the lifecycle of the product.

Develop the product requirements based on customer and patient insights, needs and business aspects and follow them throughout the product development process.

Owns the product value proposition and associated claims. Develops the product marketing toolkit including educational, sales and marketing tools.

Perform business intelligence, market & competitive analysis and translate them into actionable business goals.

Develops global go-to-market strategies in collaboration with regional teams (segmentation, targeting, positioning, pricing) to drive market share and profitable growth.

In cooperation with the Clinical department, developing educational tools and programs for customers on the clinical value and product use to drive adoption of our offering in the field.

Coordinating the assigned products activities in a multi-functional organization; including marketing, sales, operations, engineering, and services teams, while ensuring compliance with quality systems and regulatory requirements.

Take an active part in the strategy and roadmap discussions of new product introductions.

Be the Product Champion! Instill a sense of excitement about our products within the organization, and the relevant community as a whole.

you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. Youll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life
you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. Youll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
leading Medical Device company and searching for an Operations Quality Assurance Manager to lead quality operations team in Yokneam site. In this role, reporting directly to the EMEA Sr. Operations QA Director, you will manage team of Quality engineers conducting professional quality assurance procedures, in the field of endoscopy products and lead a site QMS strategy. The position is on-site, travel may be required up to 10% of the time.

Responsibilities may include the following and other duties may be assigned:
Act as Quality Management Representative.
Responsible for the Yokneam site quality management system.
Develop and implement a comprehensive QA strategy aligned with the company's overall goals and vision.
Ensures the quality assurance programs and policies are maintained and modified regularly.
Build and develop the capabilities of the quality team, fostering a culture of continuous improvement, innovation, and collaboration.
Implement Lean, Six Sigma, or other quality improvement methodologies.
Update company management on quality performance and policy implementation.
Responsible on MRB activities, periodic quality reviews, and provide actionable insights.
Responsible for CAPA management and risk assessment.
Co-ordinates legal requests in support of government investigations or litigations
Lead and ensure company compliance with quality standards and certifications as required.
Leads audit and inspection preparation, resolution of audit and inspection findings and liaises with auditing groups and inspectors through all stages of the audits.
Collaborates with cross-functional resources to achieve desired results.
Understand and operate according to medical device regulatory guidelines (GMP, FDA, ISO13485, AIMD R-PAL) and company Quality System procedures.