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משרה בלעדית
1 ימים
דרושים בריקרוטיקס בע"מ
Job Type: Full Time
A global leader in medical device micro-manufacturing is seeking a Senior Manufacturing Engineer (NPI) to bridge R&D and Production. In this role, you will lead process transitions (from validation to commercial scale), drive process optimization using DFM and Lean Six Sigma, and develop automated/fixture solutions for high-volume manufacturing.
Key Responsibilities
Process & Layout Design: Design and optimize manufacturing processes, equipment layouts, operational sequences, and production workflows.
NPI & Transfer: Lead NPI projects from concept to full production, working closely with R&D, Production, and customers.
Validation & Quality: Execute process validations (IQ/OQ/PQ/TMV, Gage R&R), draft PFMEAs, control plans, and define inspection methods.
Documentation & CAD: Write work instructions, update BOMs/routers, and finalize tooling documentation using SolidWorks.
Requirements:
4+ years of experience in Manufacturing/Process Engineering.
B.Sc. in Mechanical Engineering or a relevant field.
Proven experience in Process/Product Transitions & Validations (Medical Device / Process Industries preferred).
Hands-on experience with project costing/budgeting and statistical analysis for equipment validation.
Strong problem-solving skills and fluent English (written & spoken).
Pluses: Six Sigma Green Belt, ISO 13485 Lead Auditor, Tooling/Laser/Vision systems experience, or PMP.
This position is open to all candidates.
 
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לפני 8 שעות
Job Type: Full Time
A medical device company is seeking to hire a Quality Design Assurance Engineer to join our QA team. As a Design Assurance Engineer, you will lead all quality elements of Design Controls and product DHF for new product introductions and sustaining/design projects.
Responsibilities
Quality responsibility to verify that the design and development process follows the procedures and design and development plans.
Work closely with R D and TEST teams to support regulatory requirements by creating, reviewing, and providing quality and compliance input to the design and development process, deliverables, and requirements.
Participation in project meetings to review and help update clear and concise user requirements, product specifications, plans, verification and validation studies, risk management files, and other relevant design control deliverables.
Quality responsibility for transferring
Requirements:
At least 2-3 years of experience working in a quality function in the medical device industry - must.
At least 1 year of experience as a design control engineer (preferred).
Prior hands-on experience in Verification Validation (V V) activities within the medical device industry - a significant advantage.
A Bachelor of Science in Engineering, Sciences, or a related field - must.
Familiar with statistical techniques used in verification and validation processes - must.
Experience with ISO 14971, 21 CR 820, ISO 13485, EU MDR, IEC 60601-1, IEC 62366, and IEC 62304 standards - must.
Strong analytical and problem-solving skills, with keen attention to detail.
Excellent communication and interpersonal skills, with the ability to collaborate effectively across functions.
Proficient use of standard MS Office applications.
Fluent in English (oral and written
This position is open to all candidates.
 
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חברה חסויה
Location: Haifa
Job Type: Full Time
Required Advanced Manufacturing Engineer
Role Summary
The Advanced Manufacturing Engineer (AME) is responsible for industrializing and sustaining complex PET and SPECT imaging products at a high‑complexity electromechanical manufacturing site. The AME ensures robust manufacturability of high‑level mechanical assemblies, electronics integration, wiring, detector modules, motion systems, and system‑level testing. The role drives process development, tooling, validation, DFM/DFA, quality improvement, and readiness for production and NPIs.
NPI Leadership for PET & SPECT Imaging Systems:
Lead manufacturing readiness for new PET/SPECT products, including process layout, tooling development, and new equipment introduction.
Participate in design reviews and influence DFM/DFA/DFT across mechanical assemblies, detector modules, power systems, wiring harnesses, and electromechanical subsystems.
Translate design intent into controlled, stable manufacturing processes.
Coordinate ECO implementation and ensure smooth manufacturing release.
Assembly Process Development & Optimization:
Develop robust assembly processes for mechanical and electronic integration, alignment, torque control, and detector installation.
Define and design manufacturing jigs, tools, fixtures, and lifting/handling solutions required for large subsystems.
Lead design/manufacture of equipment, tooling, and jigs internally or via suppliers to eliminate defects.
Drive LEAN manufacturing implementation and support continuous improvement.
Conduct PFMEA for existing and new processes.
Quality & Problem Solving:
Drive product quality improvements by identifying manufacturing issues and implementing cost‑effective solutions.
Work with Production Associates to resolve manufacturing and quality problems.
Oversee corrective action implementation in production or suppliers.
Support RCA through structured failure analysis.
System Integration & Testing Support:
Support integration/testing of assembled PET/SPECT systems including calibration, alignment, motion validation, detector gain calibration, and safety checks.
Work with System Engineering to define test protocols and acceptance criteria.
Troubleshoot system issues related to electromechanical assemblies.
Validation & Regulatory Compliance:
Own IQ/OQ/PQ for equipment, tools, and manufacturing processes.
Ensure compliance with ISO 13485, ISO 14971, 21 CFR 820, IEC 60601, and internal QMS requirements.
Maintain strong documentation practices including control plans, validation protocols, and DHR/DMR accuracy.
Ensure traceability for critical parameters, torques, and calibration data.
Supplier & Cross‑Functional Collaboration:
Collaborate with suppliers of mechanical assemblies, detector modules, wiring harnesses, and PCBs.
Lead technical discussions with suppliers for tooling, process capability, and quality issues.
Train and qualify production and supplier teams on processes and inspection/assembly methods.
EHS & Plant Compliance:
Lead and support Environment, Health & Safety efforts aligned with site goals.
Ensure safe handling of large assemblies, HV systems, and radiation‑related components.
דרישות:
Drive product quality improvements through systematic problem solving.
Lead design requirements for manufacturing processes, tools, and fixtures.
Design and manufacture jigs, fixtures, and tooling (internal or supplier‑managed).
Strong experience with LEAN manufacturing and PFMEA execution.
Ability to resolve complex manufacturing and quality issues.
Leadership of NPI activities including tool development and equipment introduction.
ECO coordination and controlled release management.
Strong understanding of compliance, EHS, and regulated manufacturing.
Ability to train and qualify production and supplier teams.
Mechanical/electromechanical assembly expertise.
Experience with HV/LV wiring, detector systems, and motion integration.
Strong analytic המשרה מיועדת לנשים ולגברים כאחד.
 
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05/07/2026
Location: Haifa
Job Type: Full Time
we are looking for a Senior R&D Process Development Engineer.
As a Senior R&D Process Development Engineer , you will play a key role in a multidisciplinary engineering team driving the design, development, and launch of next‑generation manufacturing platforms that enable future CT detector technologies. You will work closely with design and hardware teams to translate breakthrough concepts into scalable, automated production processes that deliver reliability, precision, and manufacturability at scale.
Your role:
Team Collaboration: Work as a key member of the R&D process team to develop, test, and implement automated assembly solutions for future products.
Process Development: design and optimization of new automatic assembly lines, specifically for high-precision CT detector modules.
Hands-on Implementation: Support the integration and fine-tuning of Die Attach systems and Epoxy/solder Dispensing processes within the R&D lab and pilot lines.
DFM Support: Participate in design reviews to provide DFM (Design for Manufacturing) insights, ensuring that new detector designs are optimized for assembly.
Technology Evaluation: Assist in benchmarking and testing new manufacturing technologies and equipment to determine their feasibility for future product lines.
Validation & Documentation: Execute DOEs (Design of Experiments) and document process characterization as part of the teams effort to meet medical regulatory standards.
Requirements:
B.Sc. in Mechanical or Materials Engineering or B.Sc. in Physics (MSc - advantage).
7+years of experience in process development of detectors assembly.
Experience working with Automatic Assembly systems.
Practical experience with Die Attach and Epoxy/Adhesive Dispensing.
Strong understanding of DFM/DFA principles.
A strong team player with an analytical mindset, comfortable working on long-term, innovative R&D projects where solutions aren't always "off-the-shelf."
Fluent English (written and verbal) for communication within a global organization.
This position is open to all candidates.
 
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16/06/2026
חברה חסויה
Location: Caesarea
Job Type: Full Time
our company, a Sisram Medical company, is a global leader in medical-aesthetic technologies, with over 25 years of experience in energy-based devices (EBD). Over the years, our company has evolved into an integrated aesthetic and wellness ecosystem that combines medical devices, injectables, diagnostics, and personalized skincare. The company operates in a dynamic, innovation-driven environment, merging advanced technology with deep clinical understanding to create holistic solutions for aesthetic clinics. our companys headquarters are in Caesarea, Israel, with business operations in more than 100 countries worldwide.
* Establish, build, and lead the V&V team from the ground up, including defining methodologies, processes, and best practices
* Manage and mentor a small and growing team of V&V engineers
* Lead end to end, comprehensive verification and validation activities for multidisciplinary medical devices, combining technologies such as laser, RF, ultrasound, and physics-based systems
*  Define, author, and execute rigorous TEST strategies, validation plans, and protocols for complex systems
* Ensure full compliance with medical device regulatory standards, including documentation, traceability, and validation processes
* Partner closely with matrixed cross-functional teams including Mechanics, Hardware, Software, system Engineering, Regulatory, Clinical and Quality
* Drive continuous improvement of TEST methodologies, modern tools, and automation capabilities
* Support end-to-end product lifecycle activities including design verification, system validation, and post-market activities.
* Partner with Operations and NPI (New Product Introduction) groups to ensure seamless transfer from design verification to manufacturing line validation
* Manage relationships and scheduling with External Certified TEST Houses for safety, EMC, and environmental compliance testing
Requirements:
* B.Sc. in Biomedical Engineering, Electrical Engineering, Mechanical Engineering, Physics, or a related exact science discipline - Mandatory
* At least 5 years of hands-on experience leading V&V / QA, testing complex multidisciplinary systems - mandatory
* Proven experience working in medical device companies - mandatory
* Direct experience with systems integrating multiple technologies (e.g., laser, RF, ultrasound, or similar physical technologies)
* Previous experience as a lead / senior role or strong potential for leadership - must
* Prior experience in building or scaling testing activities / teams - strong advantage
* Strong understanding of V&V processes within regulated environments (FDA, CE, ISO13485, etc.) - mandatory
* Deep familiarity with medical device safety and software standards, specifically IEC 60601 (Medical electrical equipment safety) and IEC 62304 (Medical device software lifecycle) - Highly Preferred
*  Hands-on experience implementing or working with Application Lifecycle Management (ALM) platforms, defect tracking tools (e.g., Jira), and TEST automation frameworks or data analysis tools (e.g., MATLAB, PythongreenTxtBg!) - Strong Advantag
*  Strong leadership capabilities with the ability to build a team and drive it forward
* Deep, fundamental understanding of system -level methodologies for complex, multi-tiered / multidisciplinary products
* Hands-on, proactive, agile approach with the ability to operate in a rapidly growing, evolving development environment
* Strong cross-functional communication and stakeholder management skills to bridge design, quality and regulatory groups
* High level of personal ownership, structure organizational skills, and uncompromising attention to detail
* Ability to balance strategic thinking with hands-on execution
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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05/07/2026
חברה חסויה
Location: Haifa
Job Type: Full Time
we are looking for a Product Quality Engineer.
Job Responsibilities:
Facilitates operations performance monitoring, reporting, improvement and development, facilitates improvement programs in factory, and supports analytical testing and Supplier Quality Engineering (SQE), Supplier Quality Assurance (SQA) and Purchasing.
Conducts assessment of impact to Process Failure Mode and Effects Analysis (PFMEA) and associated controls in relation to design changes and assists in Manufacturing Process Development and Design Transfer activities.
Leads analysis of defects for determining dispositions of non-conformances, drives management of Non-Conformances (NC) and Quality Notifications (QN) and facilitates implementation of effective Corrective and Preventive Actions (CAPA) actions.
Handles non conformance events and investigations in the factory and guides material review board activities for non-conformance disposition management.
Facilitates timely quality engineering and quality assurance tasks, ensures manufacturing quality systems are maintained, handles single or complex process validation and process improvement activities, and helps in completion of New Product Introduction (NPI) and product transfers in factory.
Possesses working knowledge of generic products/services and Quality Engineering and Continuous Improvement techniques, follows processes and operational policies in selecting methods for obtaining solutions, and frequently interacts with supervisors and functional peer groups to gain cooperation of others.
Acts as an advisor to subordinates to meet schedules and/or solve technical problems, develops and administers schedules and performance requirements, and may have budget responsibilities.
Cultivates effective relationships, demonstrating full understanding of area of specialization, demonstrates good working relationships with suppliers, and previous experience of participation in several New Product Introductions (NPIs).
Leads validation protocols, facilitates production builds to support validation activities, analyzes data for reports, process improvement initiatives, and validation activities.
Utilizes advanced statistical analysis methods to interpret complex data trends, resolve a wide range of moderate complexity requests, and provide strategic insights for continuous enhancement of quality standards and process efficiency.
Discusses detailed, strategic quality metrics and reports with stakeholders, highlighting significant achievements, emerging trends, and actionable insights to drive advanced improvement initiatives and ensure regulatory compliance.
Delivers specialized advanced training programs on cutting-edge quality standards, advanced methodologies, and best practices, fostering alignment across functions and advancing excellence in operational practices at an expert proficiency level.
Cultivates effective relationships with internal/external partners and provides influence over projects and peer groups, demonstrating full understanding of area of specialization.
Requirements:
Bachelor's / Master's Degree in Mechanical Engineering, Electronics Engineering, Science or equivalent.
Minimum required Experience:
Minimum 2 years of experience with Bachelor's in areas such as Quality Engineering, Safety Engineering, Process Engineering or equivalent OR no prior experience required with Master's Degree.
Previous experience from medical device companies- Must
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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05/07/2026
Location: Haifa
Job Type: Full Time
we are looking for a Experienced Mechanical Designer CT Detection Systems.
In this role, you will lead all mechanical aspects of the product in R&D projects, taking it from concept to full scale development while working with multidisciplinary teams that include system engineering, physics, electronics, software, project managers, and others. You will serve as a technical focal point for mechanical design decisions, balancing performance, manufacturability, reliability, and cost.
Your role:
Lead the mechanical design including 3D models, drawings, prototype manufacturing, and production transfer.
Provide solutions that optimize performance, service, manufacturability, and cost.
Perform required analysis, testing, troubleshooting, and documentation.
Work with local and global teams inside and outside Philips to answer design, service, and production challenges.
Own mechanical risk identification, mitigation plans, and design reviews.
Operate in a multidisciplinary environment under conflicting constraints of performance, reliability, cost, and development schedule.
Requirements:
B.Sc. in Mechanical Engineering
5+ years of experience in mechanical design as part of multi-disciplinary systems or products
Experience with CREO / Pro E or equivalent professional CAD systems
Experience with design of metal components and assemblies including manufacturing of high precision casted and machined parts and tolerance analysis
Experience with high standard documentation - specification documents, mechanical design documents & test protocols
Demonstrated ability to independently drive technical decisions
Highly motivated and self-driven team player
Fluent English
Advantages:
M.Sc. in Mechanical Engineering
Experience working on mechanical design of electronic components including heat transfer considerations
FEA capabilities with ANSYS Workbench Mechanical
Medical industry background
Knowledge of IDEAS
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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02/07/2026
Location: Haifa
Job Type: Full Time
we are seeking a Systems Applications Engineer to serve as a key technical resource for equipment readiness, system bring-up, and ongoing product support. In this role, you will partner closely with NPI Program Management, Engineering, suppliers, and cross-functional teams to support bills of material, evaluate design and assembly changes, ensure system and subsystem test coverage, and drive resolution of equipment issues. You will become a technical expert in prober operation and bring-up, helping ensure timely response, effective troubleshooting, and field validation of corrective actions.



Partner with NPI Program Management to understand, manage, and assess bills of material for current and future equipment configurations.
Evaluate BOM changes, design documentation, assembly requirements, and related technical updates to support product readiness and manufacturability.
Review system and subsystem test coverage to help ensure required tests exist, are properly executed, and support product quality expectations.
Work closely with Teradyne Engineering and external suppliers to troubleshoot current tool failures, identify root cause, and drive corrective action.
Support implementation of corrective actions and ensure appropriate field validation is completed.
Develop deep technical expertise in prober operation, system bring-up, and equipment behavior.
Serve as a first line of technical response for prober issues, ensuring timely escalation, clear communication, and effective remedies.
Collaborate across engineering, operations, suppliers, and field teams to improve equipment performance, reliability, and supportability.
Requirements:
Bachelors degree in Engineering or a related technical discipline, or equivalent practical experience.
10+ years experience supporting complex equipment, systems engineering, applications engineering, NPI, manufacturing, or field support environments.
Working knowledge of bills of material, engineering change processes, design documentation, assembly requirements, and test validation.
Strong troubleshooting and analytical skills, including root cause analysis and corrective action follow-through.
Ability to work effectively with Engineering, Program Management, suppliers, and field teams to resolve technical issues.
Hands-on experience with equipment bring-up, system/subsystem testing, or prober operation is strongly preferred.
Strong communication skills with the ability to explain technical issues clearly and drive alignment across teams.
Detail-oriented, proactive, and comfortable operating in a fast-paced technical environment.
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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חברה חסויה
Location: Caesarea
Job Type: Full Time
We are looking for Engineering Product Leader to join our team.

You will report to the Sr. Product Engineering Manager.



Location

On-site - Working daily from our office in Caesarea



What you will be doing:

Lead products deliverables and timelines. Responsible for NPI Processes of the company product lines

Lead Sustain engineering processes and provide engineering support across the company

Performing process validation for Engineering changes in the production line.

Collaboration with R&D, quality, and production depts. on a daily basis

Efficiency and improving production processes including electronic and mechanical assembly.

Participation in failure studies and problem-solving discussions.

Approving parts and components' SPEC deviations, and instructing for rework if needed

Develop and document Manufacturing, assembling & testing processes.

Ownership of the entire product, manage and lead the engineering changes of the product during its lifecycle
Requirements:
What you should have:

Mechanical / Industrial /Electronics Engineer
5+ years of proven experience as an NPI or Manufacturing Engineer
Understanding of mechanical and electrical process
Experience with cost reduction activities
Self-motivated, independent, and problem solving oriented
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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05/07/2026
חברה חסויה
Location: Haifa
Job Type: Full Time
We are looking for a System Engineer to join our CT (Computed Tomography) R&D team within the department. You will be responsible for gathering, analyzing, and reviewing system-level and sub-system requirements, coordinating system partitioning and total system integration using systems engineering practices.
Your role:
Contribute to system architecture, design, and integration of a complex CT subsystem.
Perform hands-on lab work, including system bring-up, debugging and root-cause analysis.
Own and maintain system-level documentation (requirements, specifications, interfaces, design rationales).
Support verification and integration activities across multiple CT platforms.
Lead technical topics and collaborate closely with HW, SW, Mechanics, Physics, Manufacturing, Quality, and Service teams.
Support field and production issue investigations and lifecycle improvements.
Requirements:
BSc or MSc in Electrical, Mechanical, Biomedical or Systems Engineering (or related field).
+3 years of experience in system engineering or complex product development.
Strong hands-on technical experience with complex HW/SW systems.
Experience writing and maintaining clear, structured technical documentation (medical devices preferred).
Knowledge of system integration, V&V, and design control processes.
Strong communication and cross-functional collaboration skills.
Fluent in English (written and spoken).
Advantages :
Experience with CT or medical imaging systems.
Experience with field issue analysis, reliability investigations, or lifecycle support.
Experience working in a regulated environment (medical devices preferred)
Familiarity with requirements, risk management, or PLM tools.
Matlab skills
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
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05/07/2026
Location: Haifa
Job Type: Full Time
we are looking for a Product industrialization engineer.
Job Responsibilities:
Ensures the implementation of process development activities specifically tailored for mid complexity projects to streamline procedures, enhance efficiencies, and ensure optimal outcomes within the defined project scope.
Introduces Design for Lean Manufacturing (DFLM) methodologies into Product Development Lifecycle Management (PDLM) processes, ensuring thorough integration of designs, particularly focusing on mid-complexity projects, to enhance efficiency and streamline production workflows.
Aligns process and equipment capabilities with specified criteria, incorporating process requirements from product specifications provided by I&D and manufacturing requirements to ensure seamless integration and compliance.
Leads timely release of Manufacturing Bill of Materials (BOM) and routes Master data, facilitating seamless integration of product specifications and ensuring efficient execution of manufacturing processes.
Oversees the implementation of complex processes and standards and ensures strict adherence to safety, regulatory, and environmental requirements, alongside local laws, company general business principles, and other relevant policies.
Addresses diverse complex product industrialization challenges through innovative problem-solving, exercising sound judgment in selecting methods and techniques to devise effective solutions tailored to specific circumstances and requirements.
Fosters productive relationships, disseminates expertise, and exerts influence within product industrialization project teams and peer groups, showcasing comprehensive mastery of the specialized domain.
Initiates design changes within factories and at supplier sites, guided by PDLM-managed projects, ensuring seamless integration and adherence to standards and timelines throughout the process.
Adheres to the relevant processes governing product introductions, qualifications, and releases specifically tailored for mid complexity projects.
Applies lean manufacturing principles and implements continuous improvement methodologies to enhance productivity and optimize outcomes within the production environment.
Requirements:
Bachelor's / Master's Degree in Mechanical Engineering
Minimum required Experience:
Minimum 2 years of experience with Bachelor's in areas such as Manufacturing/Operations
This position is open to all candidates.
 
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הגשת מועמדותהגש מועמדות
עדכון קורות החיים לפני שליחה
עדכון קורות החיים לפני שליחה
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