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Alma, a Sisram Medical company, is a global leader in medical-aesthetic technologies, with over 25 years of experience in energy-based devices (EBD). Over the years, Alma has evolved into an integrated aesthetic and wellness ecosystem that combines medical devices, injectables, diagnostics, and personalized skincare. The company operates in a dynamic, innovation-driven environment, merging advanced technology with deep clinical understanding to create holistic solutions for aesthetic clinics. Alma’s headquarters are in Caesarea, Israel, with business operations in more than 100 countries worldwide. · Prepare, compile, submit, and maintain global regulatory submissions. · Support regulatory activities across the product lifecycle, including new product introductions, design changes, software releases, labeling updates, and change control processes. · Perform regulatory impact assessments for product changes and ensure timely updates to technical documentation and risk management files. · Maintain regulatory records, technical documentation, declarations, and evidence of conformity per applicable regulations and standards. · Review and approve labeling, IFUs, UDI and promotional materials to ensure compliance. · Provide regulatory guidance to R&D, Quality, Operations, Marketing, and Clinical teams; · Participate in audits/inspections and interface with regulatory bodies/certification bodies as needed.

Subsidiary:
Alma LTD

Do you want to help create the future of healthcare? Our name, our company Healthineers, was selected to honor our people who dedicate their energy and passion to this cause. It reflects their pioneering spirit combined with our long history of engineering in the ever-evolving healthcare industry.
We offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally. Sounds interesting?
CEECA Radiology Solutions Partner (m/f/d) X ray, Fluoro & Mammography
Location: CEECA Zone (Remote)
We are looking for someone with deep radiology expertise who enjoys acting as an internal advisor - collaborating, guiding, and influencing through knowledge, competence, and professional credibility. This is an excellent opportunity to shape the radiology market - with a strong focus on Womens Health - across more than 30 countries in the CEECA zone.
Your Tasks and Responsibilities:
Provide expert consultation to internal teams on X ray, fluoroscopy, and mammography systems.
Advise on equipment selection, system specifications, and clinical workflows.
Collaborate closely with internal stakeholders: Country Business Managers, Business Partners, and Sales.
Support tender processes by preparing technical documentation and specifications.
Deliver product presentations, demonstrations, and specialized workshops for internal and external stakeholders.
Analyze market and competitor information to identify trends and generate strategic insights.
Collaborate with HQ on new product definitions and support product escalations.

we are a fast-growing, global leader in energy-based solutions for Aesthetics and Eye-Care. We are based in Yokneam, Israel (with offices in Tel-Aviv) with a strong business performance worldwide.
We are looking for a Clinical Manager for the Aesthetics Business Unit, which includes a broad portfolio of leading solutions in the market as well as an exciting innovation pipeline. The Clinical Manager will be responsible for pre and post-market activities for the assigned platform including: clinical requirements guiding design input, pre-clinical testing, clinical input to regulatory submissions, market conditioning for new solutions, post-market evidence generation and KOL development. The individual will serve as a major pillar in building relationships with global KOLs and demonstrating the clinical value and benefits of the solutions.
Key responsibilities:
Develop and manage clinical project plan, timelines, and budgets end to end; clinical research, through pre-clinical evaluations, clinical trials and publications, to user guidelines and post-market evidence generation.
Form and cultivate strong collaborative relationships with cross-functional partners in R&D, product, marketing, and regional teams
Coordinate internal cross-functional teams, as well as external clinical research associates, data managers, and biostatisticians
Oversee the execution of clinical studies, ensuring adherence to protocols and regulatory requirements
Lead the clinical input and support for key regulatory submissions and processes: regulatory submission clinical input, clinical validations, CER, CDP, CEP and more
Support marketing/commercial activities from the scientific/medical point of view: review and input to marketing collateral, develop white papers, active participation in scientific meetings and more
Communicate project status to stakeholders and provide updates on milestones and deliverables
Identify potential risks and implement mitigation strategies to ensure project success.

We are looking for a clinically minded professional with experience or interest in aesthetic treatments and beauty technologies to help evaluate, demonstrate, and communicate the performance of our innovative aesthetic devices.
This role combines hands-on product efficacy and usability evaluations and testing, oversight of external clinical evaluations, and translation of results into compelling, evidence-backed product claims.
While formal clinical efficacy evaluations are conducted by third-party partners, the Clinical Applications Specialist will also lead in-house product performance validations using tools such as VISIA skin imaging systems and other skin analysis technologies to guide the development process of our next generation aesthetic devices. The goal is to ensure our devices demonstrate consistent, measurable results throughout development and to generate supporting data for product sales materials.
Key Responsibilities
1. In-House Product Testing & Efficacy Validation (Hands-On)
Plan and execute in-house clinical efficacy validations using skin analysis tools (e.g., VISIA or similar imaging/measurement systems)
Design practical product validation approaches, ensuring repeatability, accuracy, and meaningful endpoints
Document and track testing results and participant data
Analyze results and produce clear reports, visuals, and key insights for internal decision-making
Work with R&D and Product teams to maintain clinical efficacy across development and provide feedback for improvement
2. Oversight of External Clinical & Consumer Studies (Vendor-Managed)
Define evaluation requirements and intended claims, then work with external labs, dermatologists, or research partners to design the testing plan
Review and approve third-party proposals, ensuring the scope and methods support real-world product use and claim needs
Follow up during study execution via check-ins, milestone reviews, and data snapshots
Review and assess final results to ensure data quality and relevance
3. Evidence Generation & Claims Support
Translate internal and external tests results into clear, accessible messages for sales teams, distributors, and customers
Work with Product and Marketing to create evidence-backed claims, infographics, visuals, and storytelling
Ensure consistency between clinical findings and commercial messaging
4. Training & Clinical Communication
Deliver product demonstrations and training sessions to internal teams, distributors, and aesthetic professionals
Develop training materials that use validation data in a clear, credible way
5. Cross-Functional Collaboration & Practitioner Feedback
Serve as a point of contact for partners, KOLs, and testing partners
Gather user feedback and incorporate insights into evaluation plans or product improvements
Work closely with R&D and Product teams to ensure alignment between testing, development, and launch needs
6. Scientific Awareness
Conduct focused literature reviews to support product rationale and claims
Stay informed about aesthetic device trends, skincare science, and relevant testing methodologies.

Skincare technology expert Pollogen is a dynamic subsidiary of our company, a global pioneer in energy-based technology for the aesthetics and vision domains with sales in nearly 100 countries, a large and growing installed-base, and strong presence in the US, Europe, and Asia. Pollogen offers a fresh approach to innovation, specializing in professional-grade and home-use devices that provide real results. Combined with our companys six decades of market leadership, 330+ patents, 500+ clinical publications, Pollogen and our company offer the perfect balance of scientific artistry and creative excellence.
Responsibilities
Own the full product lifecycle: market research, ideation, definition, development, validation, launch, and post-launch optimizations.
Define product requirements and translate them into clear PRDs and specifications for R&D and mechanical/electrical design teams.
Collaborate with clinical and regulatory affairs to support validation studies and submission processes.
Monitor industry trends, competitor activity, and customer insights to drive continuous product improvements.
Serve as the central point of contact for product-related decisions, balancing input from multiple stakeholders.
Ensure products meet performance, safety, and compliance standards across global markets.