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In this fully onsite role, the Manufacturing Quality Engineer will own all qualiy activities at one of the manufacturing sub-contractors, support the validation process to the contract manufacturing and provide quality oversight to the engineering department, while working within a multi-functional team environment for medical devices. The Manufacturing Quality Engineer will lead projects and tasks, from product validation through transfer to the production and play an active role to ensure products meet quality standards consistent with internal procedures and acceptance criteria. Additionally, this role will identify and implement improvements to the production processes. The Manufacturing Quality Engineer will be the products and production focal point for our sub-contractors and will be responsible for projects related to the production and machines, including training, audits, stop and renew the production.

Essential Duties and Responsibilities
Exhibit a strong quality first mentality and ensure that product and quality are held to the highest standard.
Work cross-functionally with individuals or extended teams to provide guidance and ensure success of projects.
Responsible to write, review and approve pilot documents (including reports).
Write and approve various department and production procedures and forms.
Lead investigation processes for deviations and nonconformities in production and create analysis reports.
Responsible to train the sub-contractors according to QA procedures and VoE.
Support special processes such as sorting or rework in production.
Own all production activities at one of the subcontractors to ensure manufacturing is held according to West procedures and GMP/GDP standards
Responsible for stopping and renewing production with accordance to West requirements and with MQ manager approval.
Manage production related projects and act as MQ focal point in various internal and external projects- such as Data Integrity, CoPQ, production improvement plans, etc.
Provide Quality oversight of validation activities and processes.
Lead pilot processes that include change and approval of quality aspects in pilot protocols and reports and assure that pilot processes are conducted according to West guidance and protocols.
Attend production pilot meetings as the MQ focal point.

This role is located in Shlomi, Israel and must live close to the site to be considered. This role is a hybrid model (3 days on-site/2 remote) However, during onboarding and when required, will need to be onsite.





This fully onsite role will assist in the application of manufacturing systems as well as maintain current systems in the manufacturing process to improve process control and finished goods quality while maintaining high standards of quality and safety on all phases. Provide technical assistance to the manufacturing engineering team, Quality, Global, and production as needed.

Essential Duties and Responsibilities
Ability to specify, test and design machine systems and components, including the ability to write and revise software configurations.
Support lean manufacturing initiatives, identifying reduction opportunities through process improvements, tuning of configurations, or other strategies. Improve the speed and reliability of vision system change-overs.
Responsibility for engineering projects as assigned, allowing the achievement of maximizing output and / or minimizing cost by either the implementation of new equipment and / or methods or the improvement of existing equipment and / or methods.
Plan, schedule, and perform sub-project details; follow-up on new and revised improvements to assure proper implementation.
Support and operate as needed within approved time schedules and project budgets.
Assist coordination of testing new systems before release to production.
Consult and cooperate with corporate / customer / supplier personnel as authorized and required. Maintain effective communication and working relations.
Keep team advised of any unusual situation, which might require additional attention from the project group so that they may act accordingly.
Assist newly trained West Pharmaceutical Services personnel in the use of any special equipment required for project completion.
Provide engineering guidance to assure plant, machinery, and processes are optimized.
Aid in electrical, electronic, mechanical, pneumatic, and hydraulic design modifications.
Help define projects via specifications or drawings before releasing to a vendor.

In this internship role, you will be involved in engineering activities such as issuing technical documentation, supporting equipment validation, production floor supporting and more.

Essential Duties and Responsibilities
Tech Office activities such as Documentations and Drawings.
Supporting Tooling and production processes enhancements (Automation, Jigs and Fixtures- design and built).
Supporting West IL engineers with Equipment and processes qualifications including, documentation, validation support on site, coordinate activities with subcontractors and additional tasks as assigned.
Sustain engineering support for production processes (Machines Maintenance, repairs, spare- parts and enhancements).
Additional Responsibilities
Follow Lean problem-solving techniques.
Some flexibility in schedule is required as needed for new facilities / equipment installation.
Other duties as requested and/or assigned to support the Manufacturing Engineering department.

we are seeking a Vice President, Global Project Delivery to lead and continuously evolve our global, end-to-end project delivery ecosystem across all regions and delivery models.
This executive role is accountable for defining and governing our companys delivery methodologies, standards, tools, and professional practices, ensuring consistent, high-quality execution worldwide.
While the role does not hold end-to-end accountability for individual customer projects, it is fully accountable for the maturity, scalability, and effectiveness of our companys global delivery capability.
Scope of Delivery
The role covers end-to-end customer solution delivery, including:
Complex HW + SW solutions, network elements, systems integration, and field deployment
Multi-site, multi-country delivery programs involving manufacturing, logistics, installation, integration, and customer acceptance
Delivery models spanning direct, partner-led, and hybrid approaches
Pure software-only delivery backgrounds are not considered sufficient for this role. Proven experience delivering complex technology solutions that combine hardware, software, and services is required.
Key Responsibilities
Own and continuously evolve our companys global project delivery methodologies and lifecycle frameworks
Define and govern delivery standards, tools, KPIs, and reporting models across all regions
Lead global delivery governance, maturity, and best-practice forums
Drive consistent adoption of delivery practices and professional standards across regions and delivery teams
Identify systemic delivery risks and lead cross-regional improvement initiatives
Partner closely with Regions, Product, Operations, Sales, and Support functions to strengthen execution
Serve as our companys senior authority on delivery standards, governance, and delivery professionalism.

In this onsite role, the Team Leader Quality Operations leads a team of Quality Engineers that support manufacturing processes and projects, as well as provide quality oversight to the Engineering department within a multi-functional team environment for medical devices. This Team Leader will lead QEs, projects and tasks, from product inception through commercial product and play an active role to ensure products meet quality standards consistent with internal procedures and acceptance criteria, while meeting all applicable regulatory requirements. Additionally, this role will identify and implement improvements within the Quality Management System. The Senior Quality Engineer will be a strong advocate for product, process, and system quality at all stages of manufacturing processes.

Essential Duties and Responsibilities
Exhibit a strong quality first mentality and ensure that products, processes and quality are held to the highest standard, adhere to all company policies, KPIs and follow all safety rules and safety procedures
Lead QEs daily activities, provide support, guidance, set objectives, monitor performance, and follow-ups as required.
Provide guidance on documentation structures and format to ensure compliance to procedures, relevant regulations and standards.
Responsible to provide support to manufacturing related processes, such as (but not limited to) approval of equipment qualification, process risk management and pFMEA, and process validation documents (URS, IQ, OQ, PQ, etc.), and responsible to review, and approve product development DHF documentation (product specifications, design verification & validation activities, FMEA risk documents, test methods, protocols, reports, OOSs, product transfer to operations, etc.) in relation to medical devices.
Lead the Quality involvement in development and maintenance of product and hazard analysis in accordance with West policies and procedures.
Provide Quality oversight of qualification/validation/review and approval of documentation and reports/design controls activities to other QEs
Work cross-functionally with individuals and project or extended teams to provide guidance and ensure success of projects.
Responsible to review and approve process development QMS procedures and work instructions and support QMS activities as required.
Liaison with company and customers on Quality matters related to engineering projects.
Support routine sterilization validation monitoring activities.

We are seeking an Engineering Manager for Cloud Security Product Group.

We're extending our mission of "stopping breaches" into the public cloud and cloud-native workloads. Our product offering will give customers the ability to monitor and track their cloud-native workloads as well as hardening and protecting them against attacks prior to deployment.

This offering will help with defending against potential adversary activities involving cloud-native resources. When coupled with Falcon, our endpoint security offering, our CSPG offering will provide a more comprehensive perspective on how the adversary is targeting key customer infrastructure. Our ultimate goal is to provide a single platform for securing the entire lifecycle of cloud workloads and cloud security posture.

This role is hybrid, on-site at TLV office. Candidates should be comfortable visiting the office at least 3 times a week.


What You'll Do:

Lead, mentor and grow a team of backend engineers, driving product vision and roadmap while remaining hands-on with code and architecture.

Lead backend engineering efforts from rapid prototypes to large-scale applications across our products.

Leverage and build cloud-based systems to detect targeted attacks and automate cyber threat intelligence production at a global scale.

Balance hands-on technical contributions with people management responsibilities.

Brainstorm, define and build collaboratively with members across multiple teams.

Drive technical direction and make architectural decisions for the team.

Work in a startup-like environment with a small fast-moving team.

Mentor and be mentored by other developers on backend, and data storage technologies and our system.

Constantly re-evaluate our product to improve architecture, knowledge models, user experience, performance and stability.

Be given the autonomy to own your work in a high trust environment.

In this role, you will be integrated within the Lab Engineering team in WIL R&D Lab, reporting to the Lab Engineers Supervisor and dotted line to the Lab Technicians Supervisor. You will be supporting routine WIL R&D Lab activities as part of applicable project requirements in West. You will support ongoing lab testing deliverables including reviewing the obtained results in Lab environment in compliance with GDP (Good Documentation Practice) guidelines. In addition, you will perform various testing per provided guidance to support various West platforms and products throughout product lifecycle. As part of this role, you will be able to work with different testing Equipment types, handling with calibration requirements and working with consumables, drug products and other goods.

Essential Duties and Responsibilities
Supporting ongoing lab testing deliverables including reviewing the obtained results in Lab environment in compliance with GDP guidelines.
Performing various lab testing utilizing lab equipment per provided guidance to support various West platforms and products throughout product lifecycle.
Working with dedicated digital SW (such as LIMS) as well as hard copy formats
Assist the Lab engineering team in issuing testing related documentation including results analysis.
Assist the Lab engineering team in the development of test methods, work instructions, and other as required.
Participates in the execution of Gage R&R and qualification of engineering test fixtures, assembly fixtures, test methods used in the development process of medical devices.
Working according to Lab procedures following Good Laboratory Practice and Good Documentation Practice.