דרושים » ייצור ותעשייה » Warehouse Quality Inspector (South)

Requirements:
What youll need (Required):

2 years of experience as Quality Control.

Performing measurements with measurement tools.

Ability to use applicable tools and equipment, hand eye coordination, and high manual dexterity.

Medical device experience.

Full understanding of applicable inspection procedures.

Proficient in all inspection techniques for production inspection.

Ability to clearly describe and convey nonconformance issues, and enter them into the system.

Ability to program and contribute to the validation of automated test equipment.

Ability to provide feedback on product defects and may follow through to establish resolution.

What else we look for (Preferred):

Strong communication skills and interpersonal relationship skills

Able to read, comprehend, speak, and write Hebrew.

Good English language skills, including reading and writing.

Good computer skills, required, including working knowledge of manufacturing software

Strict attention to detail.

Must be able to work with minimum supervision.

Work in a Team environment, and may work on inter-departmental teams

Adhere to Edwards Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing.

Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control.

Requirements:
Matriculation certificate or equivalent, technical background / technical courses - an advantage.
Experience in product testing and production process - a significant advantage
Ability to read and interpret work instructions and test electronic components.
Ability to concentrate and pay attention to small details for accurate data acquisition.
Ability to work with magnifiers or microscopes to see small items.

Requirements:
Bachelor's degree
A high level of English proficiency (both written and verbal) - must
Creative thinking
Strong analytical skills and attention to detail
Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams
Ability to develop and deliver training programs and support materials
Strong problem-solving skills and the ability to develop and implement effective solutions
Strong project management skills and the ability to manage multiple projects simultaneously
Experience in similar positions - a plus.

Requirements:
2-3+ years of hands-on experience in QA/RA roles within a medical device or SaMD companies.


Fluent English (written and spoken).


Proven experience with SDLC. Familiarity with design control documentation such as ECOs, PRS/SRS, RMF, STD/STR, TRA, SVD, DHF etc.


Familiarity with ISO 13485, IEC 62304, ISO 14971, 21 CFR Part 820, CE, MDR etc.


Strong attention to detail and excellent documentation practices.


Ability to work independently, take initiative, and manage multiple QA/RA processes.


Strong interpersonal and communication skills, with the ability to collaborate across teams.

Requirements:
Ability to perform repetitive and meditative work.
A high level of English proficiency (both written and verbal) - must
Eager to learn and get to know the Data world in a high-tech company.
Efficient and have good concentration skills.
Ability to take initiative, work independently and manage task without constant supervision.
Problem solver.
Strong analytical skills and attention to details.
Ability to work in a team and communicate efficiently with manager/team members.
Ability to develop and deliver support materials.
Strong project management skills and the ability to manage multiple projects simultaneously.

Requirements:
What youll need:

Bachelors degree in Science / Technology / Engineering / Equivalent.

3+ years of relevant experience in medical device industry.

Deep, expert-level understanding of Quality processes within the medical device industry.

Experience in manufacturing activities and QMS.

Demonstrated ability to manage teams, provide coaching and feedback.

Technical understanding- to allow problem solving approach in MFG line.


What else we look for:

Experience in corporate/international companies.

Management of team and sub-teams up to 5 employees.

Excellent documentation and communication skills (written and verbal), in both English and Hebrew.

Strong interpersonal skills and the ability to build effective working relationships.

Proven problem-solving, organizational, technical, and critical thinking abilities.

High attention to detail, strong execution capabilities, and effective prioritization skills.

Requirements:
* Minimum of 5 years of experience in Quality Control – mandatory
* Ability to read and interpret specifications and technical drawings (Hebrew/English) – mandatory
* Experience with RF systems – a significant advantage
* Certification in IPC-A-610 / IPC-620 – an advantage
* Familiarity with quality standards such as ISO 9001, AS9100 – an advantage

Requirements:
Electrical engineer/technician with at least 5 years of experience in testing with electronic weapons and visual inspection
Familiarity with a variety of advanced measurement tools.
Familiarity with ISO 9001, AS9100 quality standards Certification for IPC 610/620 standards
Fluency in English/Hebrew - mandatory.

Requirements:
Proven work experience as a Quality Assurance Specialist or similar role.
Writing STDs and case studies.
Working knowledge of tools, methods and concepts of quality assurance.
Solid knowledge of relevant regulatory standards.
Good communication skills, both verbal and written.
Excellent data collection and analysis skills.
Strong attention to detail.
Relevant training and/or certifications as a Quality Assurance Specialist.