לוח משרות דרושים רפואה ופארמה במרכז

As a product Manager you will be responsible for full management of the commercial aspects of the products- strategy, budgeting, business plan, including its execution and checking if it meets its target. Working closely with overseas partners, having an in-depth understanding of the field and KOL's.

The role combines working in the field and office, and cross country and overseas travel when necessary.

Responsibilities
Collect in-field, cross functional and market analysis data and synthesize insights and stakeholders behavior and drivers

Work with cross-functional team to build strategic business cross-functional plan based on strategic objectives and define KPIs

Build a tactical plan including innovative tactics and omni-channel plan to meet strategic objectives.

Execute tactical plan according to KPIs, objectives and timelines.

Prepare & execute a budget plan.

Build and manage territory plan.

Develop marketing material for in-field use in collaboration with partner and according to local regulatory requirements.

Working with medical manager to analyze scientific data and present to stakeholders.

Troubleshoot, and objection handling.

Work in accordance with the company code of ethics and guidelines laid down by the regulatory department.

Work with internal team to find solutions in order to get things done in simplified way.

Business meetings with overseas partners, training sessions, conferences, etc.

Participation in conferences in Israel and abroad according to strategic priorities.

We are looking for a Senior Pathologist to join our team.
As an part-time \ in-house pathologist, you will work closely with our R&D team on new applications for our cancer diagnostics platform as we expand it to additional tissues and indications, acting as subject matter expert and advising on all clinical matters.
You will further work with our AI experts, scientific researchers and other pathologists on tasks such as:
Annotate (mark and label) various cell types and structures in whole-slide images
Analysis of algorithmic performance and clinical data
Design and execution of clinical research and case studies
Advise on improvements to our platform, workflow and user-interface
Writing clinical, scientific and other pathology-related papers
Help the commercial team engage physicians and improve adoption of our solution by customers.

We are looking for a highly motivated and driven product manager, willing to take the next step in their career and in the world of product management, working at a multi-disciplinary environment in a fast growing and innovative company.
In this role, you will:
Be a part of the global portfolio team, reporting to the scanners segment Product Management Director.
Build the roadmap for continuous improvement of the scanners family of products, both Software and Hardware, to increase customers satisfaction, improve business performance and ensure competitiveness.
Drive customer-centric state of mind by communicating and building rapport with customers as required, ensuring the voice of the customer is reflected inside the organization.
Collect customers feedback to identify pain points and needs.
Translate customers needs into product requirements.
Guide and work with Multi-functions including R&D, Operations, RA/QA etc. developing high quality features and product improvements, delivering the roadmap goals.
Work with customer success and engineering teams to prioritize and define content for Install base quality improvements.
Serve as the global organizational focal point for the existing products portfolio.

We are looking for a Design Quality Engineer.
The Design Quality Engineer is responsible for driving exceptional product quality for the patient safety, customer value beyond expectations, regulatory assurance, and optimized Cost of Quality for the Company. This is a key technical position, affecting part quality for both installed base and NPI products.
AS a Design Quality Engineer (DQE) you will plays a crucial role in ensuring the safety, efficacy, and regulatory compliance of medical equipment including cooperated with the design and development team, and apply quality management principles throughout the product life cycle.
DQE's main responsibilities include:
Review design documents and specifications, to ensure that they meet relevant standards and regulations
Participant in risk assessment, identify and reduce potential risk quality
Take part in the design and verification process