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healthier environment and planet through our sustainability efforts.

JOB SUMMARY:
Leading and participating in Engineering procedures and activities, such as leading Lean Manufacturing processes, manufacturing equipment validation, maintenance and enhancement of manufacturing processes Engineering documentation Management, NPI projects and more.

Essential Duties and Responsibilities:
Knowledge transfer and updating from R&D to Production Floor, for new products, new manufacturing process, new equipment, machines and injection molds.
Lean Manufacturing, Productivity and process, products cost reduction.
Supporting West Pharma IL manufacturing, quality control and Regulatory activities (machines related product and malfunctions analysis and repair).
Sustain engineering support for all production processes (Machines and Molds Maintenance, repairs, spare- parts and enhancements).
Tooling and production processes enhancements (Molds, Automations, Jigs and Fixtures- design and built).
Product Engineering Industrialize and Scale- up to mass production- projects managements (machines characterizations, Projects Follow- Ups: DR's, Acceptance tests, installations, Qualifications- Verification and Validations).
Documentation and Tech Office Management- (for ex. Validation protocol and reports, SOPs, pFMEAs URS and more).
Equipment and process validation and qualifications for West Pharma IL production lines.
Product Support engineer at production floor.

We are seeking a talented Site Reliability Engineer to join our team in Israel.
Our SRE team is responsible for the design, creation, and maintenance of a complete multi-on-prem and cloud applications, deployment and monitoring framework, working with all major cloud providers. (AWS/Azure/GCP).
This is an amazing opportunity to work with a world-class technical team and to hold responsibility for designing, creating, and provisioning infrastructure as well as deploying and maintaining applications with a focus on infrastructure as code.
We aim to adopt the best solutions to fulfill our requirements, and you will be encouraged to bring your ideas and new thinking.
So, if you want to grow with us and work for a world leader company, Now it is the right time to join.
What You'll Do:
Site reliability engineer is what you get when you treat operations as if its a software problem. Our mission is to protect, provide for, and progress the software and systems behind all of our services
Ensure high uptime and reliability of Crossixs production environment, on-prem and cloud
Take responsibility for managing the production environment, security, change management, deployment, architecture, and tools
Lead technical calls with business partners to explain how our applications are architected, understand requirements, and handle production problems
Perform root cause analysis for complex failures and offer modern solutions and tools
Utilize Grafana to develop effective dashboards that provide key insights and system performance
Analyze performance and stability issues and create in-house automation tooling
Work closely with DevOps, R&D, product, and integration managers to enable automated CI/CD methods
Design, develop, and drive troubleshooting & mitigation tools as part of driving self-healing agenda
Constantly improve the technology stack, supporting the data growth
Working in a data-driven company with cutting-edge environments that combine on-prem and cloud technologies.

Required Senior DevOps Engineer - Data Platform
The Role:
We are operating and building a data platform that allows the processing of huge amounts of medical data while preserving patient privacy. To achieve that goal, our systems are deployed with multiple leading data providers in a variety of cloud and on-prem environments with unique security requirements. We are looking for a Senior DevOPs engineer who will assist us to ensure a smooth deployment and operation, complying with strict standards and adherence to best industry practices and with a potential and desire to own production systems and to perfect it.
What You'll Do
Work with Product, R&D, and integration teams to define and implement CI/CD to apply in multiple target environments for production, staging, and testing in AWS, GCP, and Azure
Assist product in gathering and generalizing requirements from business partners
Optimize environments for security, performance, and cost; optimize processes for speed
Oversee and guide the team and business partners on the implementation of best practices
Define and integrate monitoring solutions
Use tools like Terraform, Ansible, Jenkins, Kubernetes, FileBeat, OpenSearch, and other tools to set up environments in a variety of scales and security levels
Become a product deployment and operation expert.

Required Product Manager - Crossix Data Platform
The Role:
As a Product Manager on the Crossix Data Platform team, you will own the design and execution for major components of our SafeMine Cloud Product.
SafeMine Cloud is a data pipeline product that collects, matches, de-identifies, and extracts health data while maintaining patient privacy for Crossix Analytics and the Compass suite of products.
You are excited about big data and building data pipelines that deliver quality data. You are comfortable working with a cross-functional team, ranging from the Development team to peers on the Product Management and Operations team.
You will help shape the future of the product. This will include designing features, writing detailed product specifications, and working with the Development team to bring designs to fruition.
This is a great opportunity for someone who is excited about product design from the early days and thinking strategically about data pipelines and architecture for scalability, reliability, privacy, and quality in data delivery.
What You'll Do:
Own and design product features from start to finish, including user stories, functional & non-functional requirements, feature specifications, quality control checks
Manage the prioritization and focus on data pipeline enhancements
Author high-quality design specifications within an agile methodology based upon industry and downstream systems/customer requirements
Support release and sprint planning to ensure product enhancements support the needs of the internal customers at the right time and in the right sequence
Collaborate closely with Development, Data Analysts, QA, DevOps, and Product Management to ensure products are built and delivered with quality
Be accountable for the success of the product - define and analyze product metrics and quantified methodology for data quality
Acquire deep subject matter expertise in healthcare data.

Quality Engineering, Team Leader oversees projects, maintains processes and addresses quality issues by analyzing outcomes and collaborating with teams for effective resolutions. This position will continue the QA routine activities of a working WSS lab and QA duties for future business.

Essential Duties and Responsibilities
Contribute to the development and implementation of quality management programs focusing on continual improvement across various processes.
Create processes to better evaluate, track and trend audit outputs and identify risks/issues and evaluate impact on global quality systems and initiate actions, as needed.
Coordinate communication between internal teams.
Regularly analyze data trends, drive improvements and meet customer expectations through efficient reporting and communication.
Reviews, revises, and creates operating procedures to ensure compliance with all related external requirements, internal procedures or instructions, and the West Quality Manual.
Ability to lead meetings with relevant teams, employees and contractors as necessary to manage changes.
Establishes monthly KPIs and metrics to Quality Leadership.
Drive continuous quality improvement projects across the enterprise for increased compliance and to create efficient use of company resources.
Leading personnel responsible for calibration activities monitoring, calibration reports approvals. Responsible for calibration specifications approval and for reviewing and approving calibration deviations.
Lead the sites device sterilization methods establishment, validation, maintenance and routine controls as the site sterilization SME by verifying that the sterilization methods validation is done according to the applicable standards and regulations. Verify the sterilization methods and risk-based approach are routinely maintained. Address sterilization issues and provide solutions to sterilization challenges. Be a part of the West Global Sterilization Council and provide support to other West CM and Medical device sites with Sterilization issues. Be key focal point with the West IL sterilization service providers related to sterilization matters.
Independently performs supplier audits and corporate facility audits.

Travel Requirements:
20%: Up to 52 business days per year.