לוח משרות דרושים רפואה ופארמה בפתח תקווה

Medison is a distinctive global pharmaceutical company driven by an unwavering purpose: to deliver groundbreaking therapies to patients suffering from rare and complex illnesses in international markets (excluding the US, Western Europe, and Japan). Positioned at the forefront, Medison pioneers the category of multi-regional partnerships. Our collaborative efforts with emerging biotech enterprises harness the power of our unparalleled global platform. Our ultimate mission is patient-centric: to expedite access to remarkably innovative treatments for those in need. Medison embodies dynamism, rapid growth, and global presence. We seek individuals who resonate with our fervor and principles, individuals eager to unite in our mission to champion the rights of patients in distress. Operating across over 25 countries spanning 4 continents, we seek a Product Manager for the Neuro Rare Unit As a product Manager, you will be responsible for full management of the commercial aspects of the products—strategy, budgeting, and business plan—including execution and checking if it meets its target. You will work closely with overseas partners and have an in-depth understanding of the field and KOLs. 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 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