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A world-leading material science company, focused on the research, development, manufacturing, and marketing of vision and light control technologies that support safe, sustainable, comfortable, and agile user experiences across various industries.

We are seeking an experienced Chemist to join our materials team and contribute to the scale-up and pilot processes of polymers, small-molecules and nanoparticles synthesis. In this role, you will play a key part in transferring laboratory-scale chemical syntheses to production scale, optimizing chemical reactions, and supporting the development of our products from lab to pilot scale. This position requires hands-on experience in laboratory and wet chemistry development, as well as expertise in scaling up chemical processes and a deep understanding of pilot chemistry. Success in this role also depends on thriving within an innovative and collaborative team environment.

Joining the team means being part of an elite group of innovators with a passion for creating future-defining and groundbreaking technologies that shape our everyday lives.

Responsibilities
Lead and execute the transfer of chemical reactions from lab-scale to pilot and production-scale settings.
Develop and optimize scalable processes for polymers and nanoparticles, ensuring reproducibility and consistency in larger volumes.
Optimize chemical processes with a focus on cost reduction and efficiency improvements.
Collaborate with R&D teams to design and implement scale-up experiments, modifying lab procedures as needed for pilot and production runs.
Employ analytical methods, including NMR, GPC, GC-MS, rheology, and SEM, to characterize materials throughout the scale-up process.
Analyze, document, and interpret experimental data, creating detailed reports and presentations.
Collaborate closely with production teams and chemical engineers to provide support, consultation, and troubleshooting for chemical reactions.

A world-leading material science company, focused on the research, development, manufacturing, and marketing of vision and light control technologies that support safe, sustainable, comfortable, and agile user experiences across various industries.
We are seeking an experienced Quality Assurance Manager to lead our quality initiatives and ensure compliance with global standards. This role is integral to maintaining our high manufacturing standards, driving continuous improvement, and collaborating with cross-functional teams to enhance product quality and performance.
Joining means becoming part of a cutting-edge, fast-growing company that values innovation, excellence, and teamwork in shaping the future of smart materials.

Please send a copy of your CV in English.
Responsibilities
Drive quality performance and continuous improvement across the organization.
Develop and implement product quality assurance strategies across all development phases.
Define QA compliance objectives and ensure adherence to international standards (ISO 9001, VDA 6.3, IATF 16949).
Establish quality control methods, documentation, and risk management practices (FMEA, APQP, PPAP, SPC, MSA).
Investigate root causes of deviations with R&D and production teams, ensuring corrective actions.
Oversee supplier evaluations, internal audits, and customer compliance audits.
Train and supervise technical staff in quality processes, testing, and reporting.
Serve as the product safety representative and liaise with global quality teams.
Prepare for and manage internal, customer, and certification audits.
Willingness to travel internationally when required.

We are looking for a Manufacturing Engineer.
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 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 Pharma IL production lines.
Product Support engineer at production floor.

We are looking for a Quality Engineering, Team Leader.
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 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.