לוח משרות דרושים ייצור ותעשייה משרה מלאה

Requirements:
Required Qualifications:
2+ years of technical engineering experience.
OR Bachelor's degree in Electrical Engineering, Computer Engineering, Mechanical Engineering, or related field AND 5+ years of technical engineering experience.
OR Master's degree in Electrical Engineering, Computer Engineering, Mechanical Engineering, or related field AND 3+ years of technical engineering experience.
OR Doctorate degree in Electrical Engineering, Computer Engineering, Mechanical Engineering, or related field.
2+ years of experience in ASIC design and/or verification.

Other Requirements:
Ability to meet us, customer and/or government security screening requirements are required for this role. These requirements include, but are not limited to the following specialized security screenings: 
Our Cloud Background Check: This position will be required to pass the Cloud Background Check upon hire/transfer and every two years thereafter.

Preferred Qualifications:
Excellent communication skills in English.

Requirements:
What we need to see:
B.Sc. in Industrial Engineering, Manufacturing Engineering, or equivalent experience.
8+ years experience in an engineering and/or manufacturing environment in the Chip industry.
Seasoned manufacturing engineer.
Knowledge and experience in Semiconductor industry (Fabless company benefit).
Excellent skills in Excel and PowerPoint.
Performs well in an intensive and dynamic environment.

Ways to stand out from the crowd:
Vast knowledge of manufacturing processes.
Team player with good interpersonal relations.
Goals oriented meet goals and due dates.

Requirements:
At least 5 years of experience as a QMS Specialist/Eng./Manager
Bachelors degree in a relevant field, such as Engineering, Computer science, etc.
Strong knowledge of quality management principles specific to the medical device industry, including ISO 13485:2016, FDA QSR, and EU MDR (an advantage) experience with Multidisciplinary products or SaMD (an advantage).
Familiar with cybersecurity and privacy standards and regulations, such as ISO 27001:2013 an advantage
Experience working in a software company, with a dynamic environment
Certified Quality Engineer (CQE / CQM) an advantage
Certified Internal Auditor an advantage
Proven track record of communicating effectively in English, both orally and written.
Previous experience in implementing and maintaining a QMS in the medical device industry, with a solid understanding of medical device regulations and standards.
Familiarity with applicable regulatory requirements and standards, such as ISO 14971 and IEC 62304.
Strong analytical and problem-solving skills
Attention to detail and a commitment to maintaining high-quality standards
Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.

Requirements:
Ensure the proper implementation of the SDLC process according to IEC 62304, the quality of the documentation (review and approval ) in the project, that is compliance with the regulatory requirements
Support SW production/release documentation and ECO
Provide Quality support at various stages of Product Development and coaches others in analysis and decision making
Ensuring that R&D procedures and work instructions are continuously up-to-date and effective
Lead Risk Management processes according to ISO 14971
Provides the quality/independent review at defined design reviews and project design plans, for new development projects as well as design/process changes
Support the implementation of eQMS systems and quality tools used in the development process, including documentation, testing, and monitoring of the product
Keeps up to date on all ISO/FDA/MDR and other Product Development related regulatory requirements and relays this information to the Product Development group
Qualifications:
Bachelors degree in Engineering or related field, such as Engineering, Computer science, etc
5 years of related experience in the medical device, experience with the development of Multidisciplinary products or SaMD
Expert understanding of appropriate global medical device regulations, requirements, and standards, including Quality Management System ISO 13485/ QSR / MDR, SDLC IEC 62304, and Risk Management ISO 14971
Familiar with cybersecurity and privacy standards and regulations, such as ISO 27001:2013 an advantage
At least 5 years of experience as a QMS Specialist/Manager
Certified Quality Engineer (CQE / CQM) an advantage
Certified Internal Auditor an advantage
Project Management (development of project plans, status meetings, project reporting, etc) and organizational change movement
Ability to communicate perfectly in English both orally and in writing
Self-motivated and able to manage time working on multiple projects simultaneously
Tech Savvy Demonstrated competency in computer skills
Must be able to communicate appropriately and adequately to all management levels

Requirements:
Required Qualifications:
BSc in Mechanical Engineering, Aeronautics or Bio-medical Engineering from a leading university.
At least 4 years of experience as mechanical design / system engineer / BioMedical engineer.
Hands on experience with electro mechanical systems.
Problems solving orientation.
Team player, Highly motivated with ambitions to learn and develop.
Strong project leadership capability.
Multitasking.
Interpersonal skills and excellent teamwork - the ability to meet technical as well as human challenges.
Experience in medical devices' quality system, specifically is Risk management file and Design Inputs an advantage.
Experience in CAD tools an advantage.
Familiar with testing according to medical standards - advantage.
Good communicational skills in English and Hebrew- Verbal, writing, reading.
Good documentation skills.
Experience in EMC and Safety certifications an advantage.
Experience in Imaging / Electro-Optical systems - advantage.
Experience in a global company advantage.

Requirements:
Required Qualifications:
BSc in System Engineering/Electrical Engineering/Electro-optical Engineering/Mechanical Engineering/Bio-medical Engineering/Computer Engineering. MSc - advantage.
At least 8 years of experience in development of multi-disciplinary products, including HW, Mechanics, Software and Physics.
Experience in Tx-Rx systems and signal-to-noise design.
At least 4 years of experience in System Engineering.
Communication and technical status reporting skills
Interpersonal skills and excellent teamwork.
Experience in leading resolution of complex system issues, including hands on work.
Fluent in Hebrew and English.
Experience Electro-Optical systems - advantage.
Experience in Medical devices - advantage.
Experience in a global company advantage.
Knowledge of optics / laser - an advantage.

Requirements:
University or College studies in Electrical or Electro-Mechanical Engineering preferred, minimum Technician or engineering 3rd Level qualification required
A few years hands-on experience in a B2B, Industrial Equipment support role
Strong communication and facilitation skills with demonstrated ability to present complex technical information and issues in a user-friendly manner.
Good in spoken and written English
Excellent technical problem-solving, troubleshooting, and follow-up skills
Socially outgoing, ability to handle stress