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חברה חסויה
Location: Yokne'Am Illit
Job Type: Full Time
About the role:
we are a fast-growing, global leader in energy-based solutions for Aesthetics and Eye-Care. We are based in Yokneam, Israel (with offices also in Tel-Aviv) with a strong business performance worldwide.
we are looking for a Product Marketing 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 Manager will be responsible for driving the business growth of the assigned product portfolio and oversee the 360 product aspects of the products.
Key responsibilities:
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
Owns and leads all product aspects relating to the assigned products, from product inception to launch and throughout the commercial 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 clinical value and product use to drive adoption of our offering in the field.
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.
Requirements:
Education & Experience
Degree in Life Sciences, Engineering, or Business Administration required; MBA advantage.
3+ years of hands-on experience in global product management, leading hardware-based products from development to commercialization required.
Experience in medical devices and/or biotech, working with healthcare professionals under regulatory constraints highly preferred.
Prior work in a fast-paced startup or high-growth company an advantage.
Product & Business Acumen
Ability to quickly and deeply understand and analyze technological, clinical, and business aspects of the product. Developing compelling product narratives.
Strong analytical and problem-solving skills; proficiency in Excel or other data analytics tools required.
Experience conducting market research, competitive analysis, and gathering customer insights to define and refine product strategy.
Execution & Leadership
Experience working in cross-functional teams (R&D, marketing, sales, clinical, and regulatory) and influencing stakeholders at all levels.
Prior experience in working closely with global KOLs and distributors an advantage.
Self-starter with a proactive and hands-on approach to problem-solving.
Communication & Collaboration
Excellent communication and presentation skills, with the ability to clearly articulate product positioning complex concepts to different audiences.
Experience working in global markets an advantage.
Other Requirements
Willingness to travel internationally (~20%) as needed.
Native level English (spoken and written) required; additional languages an advantage.
This position is open to all candidates.
 
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Job Type: Full Time
we are a global leader in energy-based solutions for Aesthetics and Eye Care. With more than 1000 employees worldwide and sales in over 100 countries, we are headquartered in Yokneam and have offices in Tel-Aviv.
What makes this opportunity so BIG:
You will work with various functions to develop new products and
manage commercially available products via collaboration with Regional
counterparts, R&D, Regulatory, Clinical, and Business Development.
Heres what youll be doing:
Product Strategy, New Product Development & Product Life-cycle Management
Support product development decisions for current and future products.
Generate business plans, market requirements documents, presentations and supporting materials to align all functional groups behind a common product vision.
Lead product roadmap and planning within the category
Drive claims development for products
Understand patient experience with product portfolio
Provide portfolio scenario planning and value assessment
Conduct market research to uncover customer and business insights; translate those insights into products and programs that deliver growth for the product category
Understanding and analyzing competitive landscape
Represent the category during medical conferences, sales meetings, and customer visits
Maintain strong clinical and product knowledge; support internal and external customer education programs and product training as required Basic Qualifications
Travel approximately 1-2 trips per quarter.
Cross-Functional Team Participation & Leadership
Work closely with R&D teams to build roadmap and bring new products to market
Collaborate with clinical team on developing clinical studies, drive product and protocols enhancements and new product development
Participate in cross-functional teams to optimize future product strategy around given business needs, market needs, customer needs and technical capabilities.
Work with marketing partners to understand unique customer & business needs and ensure product requirements are aligned with global products and strategies.
Interact with Business Development team to identify acquisition, licensing and other partnership opportunities.
Requirements:
Bachelors degree required
Minimum of 5 years of relevant experience in product management a must
Previous experience in medical device, pharma, healthcare or B2B device-based products
Nice to Have
MBA in business
Bachelors degree in Science or Engineering field preferred
Experience in upstream product management preferred
New product voice of customer/market research and design experience
Cross-functional product management (ownership) experience
Knowledge of medical device industry practices, techniques and standards highly preferred
Experience working in a fast paced, global organization
Global perspective and mindset
Strong communication and interpersonal skills with experience communicating with senior leaders.
This position is open to all candidates.
 
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25/05/2025
חברה חסויה
Location: Yokne'Am Illit
Job Type: Full Time
we are a fast-growing medical device company focused on developing, manufacturing, and selling innovative devices for endovascular interventional procedures.= We are seeking a skilled and detail-oriented QA Engineer to join our team. The ideal candidate will be responsible for executing Quality Assurance activities, managing quality projects, and participating in process and product validations to ensure compliance with established standards and regulatory requirements. The QA Engineer will work closely with cross-functional teams to support quality projects, provide manufacturing support, and drive continuous improvement initiatives across the organization. LOCATION: Yokneam, Israel. The position includes the following responsibilities: SCOPE & RESPONSIBILITIES Manage ECOs: conduct risk assessment, update relevant DMR documents and carry out necessary IQ, OQ, PQ activities if required, finalization of implementation tasks. Manage DCOs in the PLM system : Write and update QA procedures to ensure compliance with quality standards and regulatory requirements. Manage NCR and CAPA processes: Lead, write and supervise the NCR and CAPA processes, ensuring timely and effective resolutions. Manage QA production activities: Provide quality support to production operations, addressing deviations and non-conformities to maintain high product quality. Ensuring Timely Resolution of Quality Issues: Promptly address all identified or assigned quality issues to prevent delays and maintain efficient operations. Participate in audits: Take part in internal and external audits, such as FDA inspections and notified body audits based on ISO13485, EUMDR, and MDSAP requirements.
Requirements:
Bachelor of Science degree or Engineering. 3-5 years of experience in medical device QA (ISO 13485, MDSAP, FDA QSR 820). Internal auditor certification- an advantage Ability to work in dynamic and multi-interfaced surroundings, micro and macro vision. Strong attention to details and Self-learning ability. Ability to manage time and priorities and work under pressure. English - high level (both written and spoken). Excellent leadership and people management skills. Service oriented. Knowledge and practical experience in Priority An advantage.
This position is open to all candidates.
 
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3 ימים
Location: Yokne'Am Illit
Job Type: Full Time
The Complaints Investigator will be responsible to Conduct costumer complaint investigations, identify root causes and issue an investigation report. Additionally support reportability assessment to the FDA.

Main responsibilities:

Conduct and lead customer complaint investigation related to mechanical issues, hardware issues, software issues, handling issues or production issues.
Work closely with the representative team in order to understand the nature of the complaint.
Work closely with SW and HW engineers, as well as the product team to determine the root cause of failure and ensure investigations are in compliance with the companys applicable policies.
Communicate and escalate investigation results and facilitate failure investigation decision process.
Provide recommendations to prevent failure recurrence and support for nonconformance/CAPA and ECO actions.
Requirements:
Bachelors degree in engineering: BSc Biomedical / Electrical / Mechanical engineering / Materials A must.
Minimum of 2 years experience as a complaints investigator or CAPA management - A must.
Proven experience in leading complaints investigations of a multidisciplinary system, preferably in the medical device industry.
knowledge of investigative and failure analysis techniques is preferred, experience in various root cause analysis method (e.g., fish bone diagrams, decision trees, etc..) and other quality tools is required.
Ability to write and communicate clearly in English, including generating and presenting well-written reports is required.
Ability to work in an evolving, challenging, multi-disciplinary environment with multiple tasks/projects.
Excellent prioritizing, organizational, and interpersonal skills.
A get-it-done attitude.
This position is open to all candidates.
 
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