Careers

job description:

Preparation of an annual sales plan and implementation of the sales strategy.

Leading and monitoring sales processes with customers and with the professional managers within the organization

Developing new opportunities with existing and potential customers.

Creating new customers

Creating proactive business opportunities on an ongoing basis

Participation and initiative in marketing operations

Requirements:

Bachelor’s degree in life sciences/biotechnology engineering/biomedical engineering.

Proven experience in medical devices sales – at least 3 years

High-level English, speaking and reading

High self-learning ability

Ability to work in a computerized, multitasking, and changing environment

Requirements:

B.S. degree or higher/ Practical Engineer
At least 3 years of experience in Medical Device
Familiarity with ISO 13485, Design controls, Risk management according to ISO 14971
Proven experience with V&V testing of a product in Medical Devices including familiarity with relevant standards and knowledge to communicate with laboratories:
EMC & Electrical Safety, Biocompatibility and Chemical Characterization,Re-processing Validation – Cleaning and Sterilization / Disinfection Sterilization, Validation (Gamma & ETO, Bioburden, Ster) Packaging, Integrity and Shelf life (Transportation, package testing requirements and microbial barrier)
English at high-level
High self-learning ability

: Requirements

Bachelor’s degree in Software Engineering, or a related field.

Proven experience in Digital Health for Medical Device products

Profound understanding of IEC62304, ISO 13485, and other relevant standards and regulations, as well as the V&V tests

Advantage: experience with submissions to FDA and/or Europe

Capabilities to work with customers, self-learning

manage projects and perform tasks with a high level of professionalism and responsiveness

.

Requirements:

B.Sc. degree or higher/ Practical Engineer
At least 2 years of experience in Quality Engineering in Medical Device
in design and development control (Design controls), including risk management according to ISO 14971
English at high-level
Ability to work in a multi-tasking and changing environment
High self-learning ability

Requirements:

B.Sc. degree or higher in Biotechnology/ Electronics/ Biomedical/ chemistry / engineering
Proven experience in Quality and Regulation Of Class II and above in Medical Device- must
Certificate of Certified Quality Engineer ICQE \ CQE- Advantage
English at high-level
Ability to work in a multi-tasking and changing environment
High self-learning ability

Requirements:

B.Sc. degree or higher in Biotechnology/ Electronics/ Biomedical/ chemistry / engineering Deep understanding in testing and validation of medical devices
Deep understanding of relevant regulations and standards such as
ISO 13485, ISO 14971, EU-MDR, 21CFR820, MDSAP
English at high-level
High self-learning ability and ability to deal with challenges
Ability to work in a multi-tasking and changing environment

Requirements:

Relevant education: Engineer / Practical Engineer / Science

At least one year of experience in Quality Engineering in Medical Device

Familiarity with ISO 13485 and regulatory requirements in US and Europe such as MDR and 21CFR820

High level of English

High self-learning ability and ability to deal with challenges

Ability to work in a multi-tasking and changing environment

Requirements:

At least 3-5 years of experience in Quality Assurance/Compliance/Laboratories QA in the Pharmaceutical industry.
Experience in  Sterile / Aseptic manufacturing- preferred

Managerial experience – preferred.

High-level of written and spoken English
High self-learning ability and ability to deal with challenges
Ability to work in a multi-tasking and changing environment

Requirements:

M.Sc. or Ph.D. degree in Life Sciences / Biology / Chemistry

Knowledge and experience in working with regulatory authorities

Proven experience in handling regulatory issues and problems

Knowledge and experience working with FDA databases

Knowledge and experience with chemical and biological drug development, with 505 (b)2 regulation and combinations

Understanding preclinical and clinical requirement for preIND

IND, NDA and/or other submissions

English at mother tongue level

Requirements

Academic in the field of Natural science / health - preference for advanced degrees
Scientific approach, scholarship, thoroughness and ability to draw conclusions from information
Ability to work in a changing and multi-tasking environment
Experience in scientific writing, editing scientific documents, protocols and preparing research plans
Practical experience of 2-3 years in monitoring research in the Pharma / Medical Device industry / CRO
Experience in locating and selecting centers, contracts, training, opening and closing centers
Experience in managing research files, submissions, and reporting to authorities
Training and motivation skills for the operation of medical staff and service providers
High level of English

Requirements:
Degree in Natural Sciences / Medicine / Biomedical Engineering

Significant experience in leading clinical trials and research management

Deep knowledge of accepted standards and procedures in clinical trials

Scientific and design capabilities, operations research, information analysis and conclusions

Abilities for drafting, writing, editing and examining clinical content

Ability to deal with service providers and lead processes

Ability to adapt to a changing and complex work environment

Ability to learn and conduct oneself independently

Excellent  English

Requirements:
Proven validation experience in the pharmaceutical and/ Medical Devices industry in the field of systems, equipment, software and process.
Experience in managing and leading projects
High level English
High self-learning ability and ability to deal with challenges
Ability to work in a multi-tasking and changing environment

Requirements:
Relevant academic education: Biology / Biotechnology / Pharmacy
Advanced degrees – a big advantage
At least 5 years experience in QA. Advantage for a QA manager position or similar managerial position.
Proven knowledge of quality management in GMP. Writing procedures, training employees, managing investigations, managing materials, certifying suppliers.
Advantage will be given to experience in:
Quality in aseptic production
Laboratory quality
high level English