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נאספה מאתר אינטרנט
4 ימים
חברה חסויה
Location: Tzafon
Job Type: Full Time
Our company Is a leading global company that develops, manufactures, and markets innovative fluid controls solutions for various industries, and looking for Process Mechanical Engineer to join our team.
Job Summary:
Responsible for manufacturing equipment, production output, quality, on-time delivery, process improvement, safety, and housekeeping in the manufacturing line to manufacture high quality products for customers with the objective of ensuring smooth business operations within department guidelines, work protocols and corporate policies.
Essential Duties and Responsibilities:
Day to Day Support Production BU Define Manufacturing File Utilization of Existing Processes Cost Reduction.
Rework and Scrap Reduction.
Problem-Solving.
Sustain Product Configuration RCCA implementation.
Yield Analysis & improvement.
Training (Supervisor).
Process Capability Analysis Tooling and fixture design, finishing processes as mechanical polishing.
Perform product functional/ system TEST and leak TEST, identify errors and conduct rework if required.
Requirements:
Bachelors or masters degree in mechanical engineering.
5-10 Years in Same Position in A Global Company.
Familiar With Semi-Conductor Industry and Specs.
Experience With CAD/CAM Systems.
Experience With CNC Machining.
Extensive Knowledge of Metallurgy and Metrology.
Electro Polishing, Orbital Welding, AFM And Other Surface Treatment Related To Stainless Steel.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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פורסם ע"י המעסיק
4 ימים
חברה חסויה
Location: Netanya
Job Type: Full Time
We are 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 Process Engineer to join our winning team! Job Description: The Production Engineer will be responsible for technical/engineering aspects of the production line performance, including design for manufacturability, production tooling, configuration management & optimization and monitoring manufacturing. The main task is to allow production of high - quality goods efficiently using GMP, Lean and other cost-effective methods. Leads engineering activity regarding Configuration management, design changes (ECO), NPI, TEST method and tooling design, monitoring and continuous improvement of manufacturing processes Leads engineering investigation and Failure Analysis activities in Operation, on component, products or process level Writing and updating Work Instructions and TEST Instructions Plan and execute process validation / jig validation Manage scrap reduction and yield improvement activity in manufacturing processes Main engineering point of contact to suppliers and vendors, considering quality of materials and manufacturing processes Supports MRB processes in Operation, assisting with issues relating to CAPAs, complaints and manufacturing support.
Direct Manager: Engineering Manager.
Requirements:
Education:
BSc. Degree in industrial Engineering, mechanics or Biomedical.
Job Skills:
o Good understanding of manufacturing processes, experience in a medical devices industry - an advantage.
o Professional experience as a process engineer with multi discipline product (experience transferring products from development to production) 3 years.
o Great problem-solving and debugging capabilities.
o Good understanding in pneumatic and mechanics- a must.
o Experience in a mass production environment.
o Professional experience with Solidworks an advantage.
o Familiarity with FDA and ISO 13485 medical device regulations an advantage.
o Familiarity with Design for Manufacturability and Assembly (DFM / DFA) is desired.
Language skills:
Good English, both written and verbal.
Personality:
o Self-starter with drive, focus, and initiative.
o Good communication and interpersonal skills- team player.
o An ability of technical leadership in matrix and changing environment.
o Capability and eagerness to engage in practical, hands-on tasks.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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נאספה מאתר אינטרנט
20/05/2024
חברה חסויה
Location: Shlomi
Job Type: Full Time and Travel Required
In this role, you will be involved in Engineering procedures and activities, such as leading Lean Manufacturing processes, Engineering documentation Management, NPI projects and more.

Essential Duties and Responsibilities:

1. Knowledge transfer and updating from R&D to Production Floor, for new products, new manufacturing process, new equipment, machines and injection molds.

2. Lean Manufacturing, Productivity and process, products cost reduction.

3. Leading large scale global and cross organizational projects.

4. Supporting our manufacturing, quality control and Regulatory activities (machines related product and malfunctions analysis and repair).

5. Sustain engineering support for all production processes (Machines and Molds Maintenance, repairs, spare- parts and enhancements).

6. Tooling and production processes enhancements (Molds, Automations, Jigs and Fixtures- design and built).

7. Product Engineering Industrialize and Scale- up to mass production- projects managements (machines characterizations, Projects Follow- Ups: DR's, Acceptance tests, installations, QualificationsVerification and Validations).

8. Tech Office Management- (Documentations, Revisions, part and Product Specifications, Drawings and SOPs).

9. Equipment and process qualifications/ enhancements for our production lines.

10. Developments of products configurations.

11. Molds Tracing and supervision.

12. Product Support engineer at production floor.
Requirements:
Basic Qualifications:

1. Education: B.Sc. Mechanical Engineering / B.Sc in a different field with a background in Manufacturing processes, Process development, project management etc.

2. Experience: at least 5 years in similar roles.

3. Fluent in Hebrew and English: Writing/ Reading/ Speaking.

Preferred Knowledge, languages, Skills and Abilities:

1. Ability to work under pressure.

2. Excellent Interpersonal relation.

3. Ability to work independently self-direct.

4. Analytical problem-solving skills.

5. Proven Technical experience and knowledge.

6. Creativity.

7. Excellence learning skills.

8. Excellent organizational skills including the ability to efficiently evaluate, prioritize and handle multiple and changing projects.

9. Experience with Windows office and Solid works.

10. Able to comply with the companys safety.

11. Able to comply with the companys quality policy at all times.

12. Relevant work history and/or experience may be considered in lieu of degree.

Travel Requirements: 1. Must be able to travel up to 25 % of the time
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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7728151
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נאספה מאתר אינטרנט
20/05/2024
חברה חסויה
Location: Shlomi
Job Type: Full Time and Travel Required
In this role, you will be involved in Engineering procedures and activities, such as leading Lean Manufacturing processes, Engineering documentation Management, NPI projects and more.

Essential Duties and Responsibilities:

1. Knowledge transfer and updating from R&D to Production Floor, for new products, new manufacturing process, new equipment, machines and injection molds.

2. Lean Manufacturing, Productivity and process, products cost reduction.

3. Leading large scale global and cross organizational projects.

4. Supporting our manufacturing, quality control and Regulatory activities (machines related product and malfunctions analysis and repair).

5. Sustain engineering support for all production processes (Machines and Molds Maintenance, repairs, spare- parts and enhancements).

6. Tooling and production processes enhancements (Molds, Automations, Jigs and Fixtures- design and built).

7. Product Engineering Industrialize and Scale- up to mass production- projects managements (machines characterizations, Projects Follow- Ups: DR's, Acceptance tests, installations, QualificationsVerification and Validations).

8. Tech Office Management- (Documentations, Revisions, part and Product Specifications, Drawings and SOPs).

9. Equipment and process qualifications/ enhancements for our production lines.

10. Developments of products configurations.

11. Molds Tracing and supervision.

12. Product Support engineer at production floor.
Requirements:
Basic Qualifications:

1. Education: B.Sc. Mechanical Engineering / B.Sc in a different field with a background in Manufacturing processes, Process development, project management etc.

2. Experience: at least 5 years in similar roles.

3. Fluent in Hebrew and English: Writing/ Reading/ Speaking.

Preferred Knowledge, languages, Skills and Abilities:

1. Ability to work under pressure.

2. Excellent Interpersonal relation.

3. Ability to work independently self-direct.

4. Analytical problem-solving skills.

5. Proven Technical experience and knowledge.

6. Creativity.

7. Excellence learning skills.

8. Excellent organizational skills including the ability to efficiently evaluate, prioritize and handle multiple and changing projects.

9. Experience with Windows office and Solid works.

10. Able to comply with the companys safety.

11. Able to comply with the companys quality policy at all times.

12. Relevant work history and/or experience may be considered in lieu of degree.

Travel Requirements: 1. Must be able to travel up to 25 % of the time.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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עדכון קורות החיים לפני שליחה
7728149
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נאספה מאתר אינטרנט
20/05/2024
חברה חסויה
Location: Shlomi
Job Type: Full Time and Travel Required
In this role, you will be involved in Engineering procedures and activities, such as leading Lean Manufacturing processes, Engineering documentation Management, NPI projects and more.

Essential Duties and Responsibilities:

1. Knowledge transfer and updating from R&D to Production Floor, for new products, new manufacturing process, new equipment, machines and injection molds.

2. Lean Manufacturing, Productivity and process, products cost reduction.

3. Leading large scale global and cross organizational projects.

4. Supporting West Pharma IL manufacturing, quality control and Regulatory activities (machines related product and malfunctions analysis and repair).

5. Sustain engineering support for all production processes (Machines and Molds Maintenance, repairs, spare- parts and enhancements).

6. Tooling and production processes enhancements (Molds, Automations, Jigs and Fixtures- design and built).

7. Product Engineering Industrialize and Scale- up to mass production- projects managements (machines characterizations, Projects Follow- Ups: DR's, Acceptance tests, installations, QualificationsVerification and Validations).

8. Tech Office Management- (Documentations, Revisions, part and Product Specifications, Drawings and SOPs).

9. Equipment and process qualifications/ enhancements for West Pharma IL production lines.

10. Developments of products configurations.

11. Molds Tracing and supervision.

12. Product Support engineer at production floor.
Requirements:
Basic Qualifications:

1. Education: B.Sc. Mechanical Engineering / B.Sc in a different field with a background in Manufacturing processes, Process development, project management etc.

2. Experience: at least 5 years in similar roles.

3. Fluent in Hebrew and English: Writing/ Reading/ Speaking.

Preferred Knowledge, languages, Skills and Abilities:

1. Ability to work under pressure.

2. Excellent Interpersonal relation.

3. Ability to work independently self-direct.

4. Analytical problem-solving skills.

5. Proven Technical experience and knowledge.

6. Creativity.

7. Excellence learning skills.

8. Excellent organizational skills including the ability to efficiently evaluate, prioritize and handle multiple and changing projects.

9. Experience with Windows office and Solid works.

10. Able to comply with the companys safety.

11. Able to comply with the companys quality policy at all times.

12. Relevant work history and/or experience may be considered in lieu of degree.

Travel Requirements: 1. Must be able to travel up to 25 % of the time.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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עדכון קורות החיים לפני שליחה
7728163
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נאספה מאתר אינטרנט
06/05/2024
חברה חסויה
Location: Yokne`am
Job Type: Full Time
Mechanical Engineer within the Urology Division will be responsible for providing support for released products within the Laser Franchise, which consists of Holmium and CO2 laser capital systems, laser fibers and associated accessories.

Mechanical Engineer works in close collaboration with the different technical disciplines (Elec, Mech, SW, Physics), as well as the other cross-functional groups (Quality, Regulatory, Manufacturing, Service) to support sustaining activities as part of Product Life Cycle.

Mechanical Engineer supports growth of products to new markets and leads design changes originating in product improvements, regulatory or supply chain needs.

Main Duties:
Conduct root cause analysis of design related field complaints.
Lead product improvement design activities.
Provide technical assistance for sales and marketing activities.
Support the integration of acquired assets within the laser franchise into the company`s Scientific quality system.
Work in collaboration with Regulatory team to provide and maintain the regulatory design inputs and systems compliance. Own the transfer from regulation/standards to engineering derivatives (impact assessment and deployment).
Support RA team with new markets registrations and regulatory submissions.
Definition, writing and management of Design Inputs and flow down for the sustaining products.
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.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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עדכון קורות החיים לפני שליחה
7711807
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נאספה מאתר אינטרנט
13/05/2024
חברה חסויה
Location: Yokne'Am Illit
Job Type: Full Time
we aim to improve patient outcomes by empowering every gastroenterologist across the globe with artificial intelligence and disruptive therapeutic technologies.

In this exciting role as an Operation Quality Engineer, you will directly support the day-to-day Yokneam products manufacturing, transfer, and improvements activities. You will have the opportunity to drive a culture of continuous improvement by deploying sound engineering fundamentals to achieve quality objectives and ultimately yielding better patient outcomes.

A Day in the Life
Communicate quality standards and requirements within the organization and collaborate with engineering and manufacturing functions to ensure quality standards are in place. Devise and implement methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment.
Oversee and participate change approval process (risk assessment, verification, validation).
Lead Quality Assurance and product quality improvements in cross-functional initiatives. Ensure that corrective measures meet acceptable reliability standards, and that documentation is compliant with requirements.
Collaborate with global Operations, QA, Engineering and Manufacturing to ensure quality standards are in place and support day-to-day manufacturing activities.
Specialize in the areas of production control, incoming material, product evaluation, and reliability, inventory control, and development as they apply to product or process quality.
Take an active role in leading and reviewing design and manufacturing changes and lead product quality investigations in support of CAPA, complaints and non-conforming material processes and lead Quality Assurance and product quality improvements in cross-functional initiatives.
Requirements:
Bachelor degree in mechanical, industrial or similar engineering disciplines.
3+ Years of Quality Assurance experience in Medical device companies or other highly regulated industries.
Strong written and verbal communication skills (English and Hebrew)
Strong knowledge of applicable standards and regulations standards (FDA, ISO13485, MDD).
Auditing experience.
Nice to Haves
Strong understanding of process validation principles, including experience with master validation plans, installation qualifications, operational qualifications, process qualifications, and test method validations.
Vast experience with design changes, change impact assessment and design transfer activities.
Certified Quality Engineer (CQE) or other similar Quality/reilibility certifications.
Six Sigma certification.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
7719810
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נאספה מאתר אינטרנט
5 ימים
חברה חסויה
Location: Yokne`am
Job Type: Full Time
We are looking for a Senior Opto-Mechanical Engineer! NVIDIA's GPUs and SOCs are the world leaders in performance and efficiency, and we are continually innovating in creative and unique ways to improve our ability to deliver extraordinary solutions in a wide range of sectors. We are seeking mechanical engineers who are passionate about what they do and are committed to making a difference in the world through their inventions. This position will collaborate with mechanical, opto-mechanical, and process engineers in the design and development of components that will drive our products into a new technology era. Your responsibilities will include designing mechanical components and assembly platforms, selecting technology, and benchmarking solutions, all while keeping schedule and budget targets.

What you'll be doing:

Development of innovative microelectronics packaging of our Networking Business Units future products.

Mechanical design and design validation of micron-scale optical elements (lenses, connectors, etc.).

Mechanical design and solution for micron-scale assembly stations.

Work with world-leading vendors to develop highly ambitious packaging solutions.

Partner with engineering to solve problems during New Product Introduction enabling an efficient transition to Mass Production.

Join and lead task forces to investigate and support production excursions, failure analysis, and reliability issues.
Requirements:
What we need to see:

BS or equivalent in Mechanical or Opto-Mechanical Engineering.

5+ years of hands-on experience with sophisticated Electro-optical or Opto-mechanical developments and manufacturing.

Proven experience in designing micron-level assemblies.

Innovative character passionate about out-of-the-box solutions for sophisticated problems.

Track record of exceptional lab work management. Results analysis, and excellent reporting methods.

Vast experience in mechanical solutions for tiny complex systems materials, heat dissipation, high accuracies, etc.

Experience with co-working with subcontractors and vendors.

Curious and creative problem solver as well as organized and multi-tasker.

Proven ability to drive and motivate direct and indirect peers. Strong interpersonal skills (verbal and written).

High awareness of quality, robustness, and manufacturability.

Ways to stand out of the crowd:

Background with opto-mechanical designs (lenses, ferrules, connectors, etc).

Experience with opto-mechanical assembly processes. Assembly jigs design.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
7736873
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נאספה מאתר אינטרנט
5 ימים
חברה חסויה
Location: Migdal Haemek
Job Type: Full Time
Key Responsibilities:
* Mechanical design: Metal &Plastics parts, Jigs & Fixture.
* Production support, subcontractors.
* PLM Support (ECO, ECR, DMR).
* Component engineering.
* NPI.
 
Benefits We Offer:
We have a real focus on developing our people, and by fostering an entrepreneurial culture, we encourage flexibility, accountability and autonomy. The company is full of opportunity for those who wish to grasp it. Our people thrive on engagement, development and a varied workload. You will often be included in projects that require you to collaborate cross-functionally.
Currency GBP
Duration
Salary Maximum 0.00
Salary Minimum 0.00
Location Israel

Job Details:
We are currently recruiting for a Mechanical Engineer at our Migdal HaEmek, Israel office.
The Mechanical Engineer will deal with a variety of planning and manufacturing issues and will be integrated into planning and development processes. The Mechanical Engineer will create product trees, production portfolios, deal with component engineering, Engineering investigation cases, accompany manufacturers and suppliers, as well as company's products throughout their lifetime.
The ideal candidate will need Mechanical Engineer BA and the ability to formulate, speak and write documents.
Location: Migdal HaEmek, Israel
About us:
Founded in 1971, we are a global medical aesthetics organisation, that delivers an extensive product range. With an in-house commercial infrastructure, including manufacturing and a network of distributors in leading global markets, our products are sold in 55 countries worldwide.
This is a great time to join us as we continue to increase our product range and expand into new markets and territories.
Our Vision:
Providing aesthetic excellence globally.
Requirements:
Description Your Skills & Experience Do You Have What it Takes?
Essential:
* Mechanical engineer-BA.
* Experience - at least 3 years.
* Ability to formulate, speak and write documents in English.
* Full control of Office applications.
* Full control of Solid works.
* Familiarity with multidisciplinary systems, electronic/mechanical hardware.
* Familiarity with Sheet metal technology, layouts, raw materials, finishes
* Good human relations, thoroughness, diligence, willingness to work hard.
* Ability to work in a team and maintain an interface with several disciplines.
* Neat and organized.
 
Desirable:
* Familiarity with printed circuit design and manufacturing technology (mechanical).
* Familiarity with metal and plastic finishing technologies
* Familiarity with quality requirements for medical products
* Introduction to the field of pneumatics
* Knowledge and experience in the E.R.P. system, PRIORITY
* Familiarity with machining technology, engraving, milling, other
* Familiarity with the design and production of injection plastic parts, raw materials
 
A bit about you do you fit this description?
* Quick learner and multitasking.
* Strong attention to detail.
* Excellent interpersonal skills.
* Quick understanding the gaps and...
* Great initiative and independence and quick response based on understanding the needs.


If this sounds like you and you meet the requirements, please apply, we would love to hear from you.
Please note if we receive a high volume of applications, we may close the role before the closing date noted.
By making this application you give consent for personal information to be used in automated decision making processes relating to key job requirements which are stated in this ad.
If you have any questions, please email us.
We do not accept speculative or unsolicited CVs from Recruitment Agencies. Any unsolicited CVs received will be treated as property of us and Terms & Conditions associated with the use of such CVs will be considered null and void.

 
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
7737527
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נאספה מאתר אינטרנט
4 ימים
חברה חסויה
Location:
Job Type: Full Time
we are looking for Senior Product Engineer to join us.
This position is a critical role that requires an individual to lead product lines throughout their life cycle. You be required to have experience in DBR (Drawing, BOM, and Routing) and possess knowledge of customers' needs, production, and process engineering, provide Failure Analysis support and lead a small team of engineers and contractors to support product development. Overall, the Senior Product Engineer is expected to be a driven individual with strong leadership skills, excellent communication, and time management skills. They must prioritize project deadlines and work efficiently to coordinate activities involving multiple areas of expertise.
Essential Duties and Responsibilities:
Supporting the companys current product portfolio and expanding portfolio as needed. Preparing product and assembly drawings using CAD software (SolidWorks).Performing tests in internal/external laboratories (investigations/validation/qualification tests for new products) Decision maker in MRB meetings Supporting Product Marketing Engineers (very technical questions). Supporting QA in investigations (internal/external). Supporting Manufacturing Engineering and assembly line. Participating in contract review meetings -- assembly /testing feasibility. Improving existing products. Leading ECR/ECO meetings.
Requirements:
Knowledge, Skills and Abilities:
Experience with CNC machining. Previous experience working with subcontractors. Proven 3D CAD experience. Knowledge of manufacturing, raw materials, finishing & QA. Ability to manage in parallel multiple tasks, projects, and co-workers. Team player, self-motivated, with strong analytical thinking. Excellent English (both verbal and written). Hands-on experience. Understanding engineering processes and proficiency in various technological fields.

Educational & Experience Requirement:
BSc degree, in Mechanical Engineering. Work Experience: 5-10 Years
This position is open to all candidates.
 
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עדכון קורות החיים לפני שליחה
7730551
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נאספה מאתר אינטרנט
25/04/2024
חברה חסויה
Location: Yokne`am
Job Type: Full Time
Highly skilled and motivated Quality Design Engineer to join our dynamic team in the medical device industry.

The ideal candidate will have a strong background in design control, quality assurance, and regulatory compliance, with the ability to work collaboratively with R&D, Engineering, Regulatory and other teams.
Adaptable and possess a deep understanding of the regulatory landscape governing medical devices, specifically experience in all phases of product life cycle (design, development, risk management, design verification, production) in adherence with ISO13485:2016, 21 CFR 820 and ISO14971.
Main Duties:
- Lead and implement design control and production processes to ensure compliance with industry standards and regulations.
- Lead proactive design assurance activities facilitating the development and release of high-quality products.
- Collaborate with cross-functional teams to integrate quality into the design and development and manufacturing process.
- Stay abreast of evolving regulatory requirements for medical devices and ensure the company's adherence to relevant standards.
- Work closely with R&D teams to understand design requirements and provide quality engineering input throughout the product development lifecycle.
- Conduct design reviews to identify and address potential quality issues early in the process.
- Responsible for reviewing, providing input and approving product development DHF documentation (design planning, inputs and outputs, design review, V&V protocol -reports, risk analysis, and design change, product transfer to operations, etc).
- Responsible for approval of product design changes and process changes (ECO).
- Participate in Design Reviews for product teams as the quality expert, reviewer, and approver.
- Implement risk management processes and methodologies in the design and development phases per ISO 14971.
- Participate in risk assessments and develop strategies to mitigate potential risks.
- Establish and maintain quality assurance procedures to ensure product quality and regulatory compliance.
- Conduct audits and assessments to identify areas for improvement and implement corrective actions.
- Conduct Failure investigations for Complaints and CAPA.
- Responsible for approval of equipment qualification and process validation documents (pFMEA, IQ, OQ, PQ, etc).
- Perform supplier audits and provided support in preparation and performance of external audits to ensure quality and regulatory requirements are met.
- Support continuous improvement activities to reduce product failure rates.
Requirements:
- Bachelors degree in engineering, preferably in a relevant field (e.g., Biomedical Engineering, Mechanical Engineering).
- Minimum of 3 years of experience in quality design within the medical device industry.
- Proven track record of successful collaboration with R&D, Engineering, Regulatory Affairs, and other teams.
- In-depth knowledge of design control processes and regulatory requirements (FDA, ISO, etc).
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal skills.
- Leadership skills without direct authority responsibility.
- Ability to present complex technical information in a clear and concise manner.
- Comfortable speaking in front of diverse stakeholders, including internal and external teams.
- Self-learning.
- Strong English capabilities.
- Demonstrate flexibility in adapting to changing project requirements and priorities.
- Relevant certifications in quality management or regulatory affairs advantage.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
7702696
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