לוח משרות דרושים מדעי החיים, טבע וחקלאות בשרון

looking for an Obesity Medical Scientific Liaison for the center-south region. In this role, you will be responsible for delivering high level medical and scientific expertise to internal and external stakeholders, within the obesity therapeutic area. You will be responsible for internal insight generation, scientific communications, and regional medical activities. In addition, you will work most of the time in the central and southern region of Israel with an 80 percent work rate in the field.
Your main accountabilities will be:
Development of professional relationships with external key opinion leaders and other stakeholders.
Leading scientific dialogue with key opinion leaders, including scientific presentations and personal meetings.
Identification of healthcare professional influencers within the obesity therapeutic area.
Drive internal and external scientific updates.
Drive local, regional, and international medical meetings and activities.
Generate insights from the field and participate in internal medical strategic planning.

As a Start-Up Team Manager, you will be responsible for executing the Start-Up team activities in clinical trials performed in Israel, ensuring compliance with local regulations, ICH-GCP, procedures and protocol requirements.
In addition, you will have the following responsibilities:
Manage and lead the Start-Up team, set and monitor performance targets and KPIs for the team and functional area in close cooperation with Israels Clinical Development Center (CDC) Director and with the Therapeutic Area (TA) Heads.
Ensure preparation and submission of local Clinical Trial Application to Health Authorities and Ethics Committees (ECs) to obtain all necessary regulatory approvals within defined timelines.
Deliver reliable, high-quality data and ensure study participants protection to activate sites prior to FPFV (First Patient First Visit) in the country.
Manage the lifecycle of clinical trial agreements/contracts, including sub-contractors, across trials.
Execute regulatory submissions of Clinical Trial Applications (CTA) and ongoing submissions and obtaining approvals.

As the Israel CDC Therapeutic Area Head, you will manage and lead the clinical research Therapeutic Area team and ensure that all clinical trial activities are carried out in compliance with all policies, procedures and local requirements.
You will also have the following responsibilities:
Ensure Clinical Therapeutic Area team set-up as per procedures and local regulatory requirements, unit processes & systems, resources and conduct of clinical trials in the CDC.
Drive implementation and execution of CDC trial delivery strategies and make sure risk plans are in place when needed in close cooperation with the CDC director.
Ensure performance management of the Clinical Therapeutic Area team, while guaranteeing the Clinical Research Unit goals are met.
Develop and maintain partnerships and effectively communicate with internal stakeholders, as well as external such as investigators, vendors, clients, KOLs, Ethics Committees and Health Authorities.
Inform internal stakeholders about trial/project related issues and the local therapeutic business scenario covering any current and/or potential changes in local trial related regulation.

ART MEDICAL is a well-funded, medical startup developing cutting-edge technologies for ICU patients. Our smART+™ platform is an intelligent, sensor-based feeding system for critical care patients that aims to prevent life-threatening in-hospital complications, such as ventilator-associated pneumonia, malnutrition, and acute kidney injury. With the introduction of Nutrition Management 2.0™ to critical care patient scoring systems, the smART+™ platform monitors, analyzes, and prevents malnutrition and gastric aspiration in real-time. By providing optimal nutritional care and achieving up to 100% feeding efficiency, the smART+™ platform improves the standard of care and helps ICU patients recover faster. As a System Engineer, reporting to The System Engineering Manager, You will be part of a multidisciplinary group of system, hardware, firmware, software and software test engineers. You will serve as an internal and external technical liaison for multiple interfaces in the organization and externally you will drive medical products into the next level of maturity and performance to meet the user and business needs. Main position duties:
* Translate user needs into actionable technical system requirements
* Manage system, sub-system and software requirements of Medical devices
* Responsibility for development of the system architecture and top-level design
* Work in a multidisciplinary and complex technical environment
* Perform risks management activities for product and production
* Act as the technical lead of multidisciplinary medical system and subsystems
* Responsibility for the system functionality, performance and quality
* Translate field and production feedback into product and production improvements
* Work closely with multidisciplinary R&D team V&V, regulatory, quality and more
* Write V&V test plans and test methods
* Participate and lead product life cycle processes
* Perform R&D projects planning and tasks breakdown

A fast-growing global medical device company, developing and manufacturing innovative drug delivery and infusion solutions across the continuum of care- from the hospital to the home. We are looking for an excellent Student to join the system team.
Job Description:
Analyze and manage risk analysis and assurance case reports for various company products
Serve as risk analysis focal point across the organization
Develop algorithms for various system components
Design and implement experiments for various projects
Participate in departmental tasks that include problem solving and critical/root cause analysis

The Senior Specialist, Quality System Engineer will ensure the West IL Quality Management System consistently meets the regulatory, enterprise and customers requirements. The Senior Specialist, Quality System Engineer will be responsible for developing and implementing continuous monitoring and improvement of the Quality Management System according to applicable regulatory requirements- MDD 93/42/EEC, Medical Device Regulation (MDR) 2017/745, 21 CFR 820, MDSAP, ISO 14971, ISO 13485 etc. and will make sure the QMS is maintained and effective . Senior Specialist, Quality System Engineer will provide support with the analysis of quality issues to identify root causes and implement corrective action to reduce risk of quality failures.

Essential Duties and Responsibilities:
The Sr. Specialist, Quality System Engineer will have an in-depth knowledge and experience of the applicable regulatory requirements and will make sure those are implemented throughout the quality management system, maintain the quality system procedures by verifying their compliance to relevant regulatory requirements, lead quality related matter regarding MDR and other regulatory requirements.
Responsible for the sites internal audit program- managing the internal audit plan as per applicable regulatory requirements, lead audits, collaborate with additional auditors, maintain the pool of auditors, review and approve audit reports, set corrective actions and perform follow ups, as well as ensure nonconformances/deviations/complaints are investigated and assessed for root cause and identification and closure of effective CAPAs
Lead and perform risk-based approach (risk assessments) processes and implement control plans.
Responsible for site improvement projects related to Quality processes such as (but not limited to- Data integrity, Lean/Six Sigma projects, CoPQ/cost reduction, etc.).
Responsible for the QA approval of employees training files and approval of employees qualification certificates.
Responsible for the sites metrics and KPI data collection and analysis, including weekly, monthly (including MBR) and routine reports, both internally and externally. Collaborate with both internal and external stakeholders in relation to metric reporting. Identify trends in applicable areas, analyze, evaluate and initiate applicable actions to mitigate, and for presenting the data during Management Reviews
Responsible for the sites procedures alignment with applicable West Enterprise procedures.
Interact and collaborate with Laboratory; Operations, Engineering, R&D, RA, D&T and other functions to support resolution of Quality issues and investigations.
Maintaining the quality system procedures by verifying their compliance to relevant regulatory requirements.
Lead the activities to Identify and verify quality agreements with Economic Operators are up to date with the state of the art EU/US and ROW regulatory requirements along with references to the applicable SKU and distribution zones to the relevant customer/EO.

We are hiring!
we are the game changer of the snacking industry. We are on a journey to take the snacking world, one category at a time.
We are looking for the right person to join our new product development team as a food Scientist, creating the next generation of snacks, all the way from lab to industrial line production.
The right person needs to have a passion for food, a good understanding of food technology basics, organization skills, and hands-on abilities that are required in our manufacturing facility.
The job includes:
       Execution of R&D projects and experiments
       Summarize and analyze trials, data and results
       Exploring new ingredients and approving raw material specs
       Examining and ensuring shelf-life
       Taking an integrative part in the transition process from lab to industrial manufacturing.