לוח משרות דרושים מהנדס כימיה

We are seeking a Project Manager with a strong chemistry or technical regulatory background to support the operational, analytical, and cross‑functional activities of the Regulatory Affairs team.
In this role, the Project Manager will lead the planning, coordination, and execution of regulatory and cross‑departmental initiatives, ensuring alignment with organizational priorities and timelines. The position requires strong project management expertise and excellent communication skills. Responsibilities include coordinating team workflows, preparing project documentation and presentations, and facilitating effective collaboration with internal stakeholders, external partners, and regulatory service providers.
Key Responsibilities:
Lead material compliance projects, including planning and execution.
Develop, maintain, and monitor project plans, timelines, milestones, and deliverables.
Track team progress, ensure follow‑up on open items, and help remove obstacles.
Assist in annual and ongoing budget planning and management.
Coordinate and collaborate with R&D, Operations, Engineering, Legal, and other teams across the organization.
Monitor, interact, report, and provide support to local R&D and Engineering regarding compliance matters, enforcement actions, remedial activities, and regulatory requirements.
Manage global initiatives, ensuring alignment and effective utilization of cross‑functional resources.
Work with advisory services and manage regulatory subcontractors.
Assess local and regional compliance requirements and implement programs/systems to ensure regulatory compliance.
Gather strategic intelligence on evolving product regulations, advise management, and drive implementation of required compliance actions.
Generate or collect necessary documentation to support certifications and coordinate submissions to certifying laboratories/organizations.
Evaluate regulatory trends and revisions, and work with functional departments to proactively adjust processes to avoid certification disruptions.
Develop workflows, protocols, and tactical direction to support standardization and administration of product compliance programs.
Ensure all stakeholders are aligned and informed of progress, changes, and dependencies.
Prepare clear, professional presentations and reports for internal and external audiences.

Required Senior Process & Yield Engineer - Manufacturing
Position Overview
The Senior Process & Yield Engineer will play a key role in developing, optimizing, and sustaining manufacturing processes to ensure quality, device performance, and line yield.
This role involves deep technical ownership of process modules, cross functional problem solving, yield excursion management, and continuous improvement of factory performance.
The ideal candidate possesses hands on process expertise, strong data driven decision making capabilities, and a proven ability to lead complex engineering initiatives in a high volume manufacturing environment.
Job Description
Key Responsibilities
Sustaining Process Engineering:
Monitor process health and equipment performance; respond to line abnormalities and excursions in real time.
Collaborate with Equipment Engineering to ensure tool matching, qualification, and tool health stability.
Maintain process documentation, change management, FMEA, and risk assessments.
Process Development & Optimization:
Develop, characterize, and optimize process steps to meet device performance, yield, and cost targets.
Own and coach DOE planning and execution to improve process stability, robustness, and manufacturability.
Define process recipes, operating windows (EWAs), and control plans aligned with technology requirements.
Yield Engineering & Data Analysis:
Conduct root‑cause analysis for yield loss and parametric drift; drive corrective and preventive actions (CAPA).
Use statistical tools (JMP, Python, SPC systems) for yield trend analysis and early detection of process anomalies.
Lead continuous improvement cycles through Six Sigma and structured problem‑solving methodologies.
Cross-Functional Collaboration:
Work closely with device engineering, equipment teams, integration, and quality to resolve technical issues.
Support NPI (New Product Introduction) activities including process readiness, qualification, and ramp to volume.
Participate in cross-site technical forums, best-practice sharing, and global engineering programs.

Landa seeks a Senior Materials Researcher specializing in industrial inkjet ink formulations. The role combines deep materials expertise with a practical understanding of complex interactions within Nanography systems, driving innovations from early research through manufacturing release.

Responsibilities:

* Development and optimization of water?based industrial inkjet ink formulations
* Design, plan, conduct, and analyze experimental work to support ink performance and reliability
* Maintain strong experimental traceability, documentation, and data integrity
* Collaborate with cross?functional teams, including jetting, process, mechanical, service, and operations
* Provide technical solutions for customer escalations related to ink performance
* Support transfer of ink formulations from lab?scale development to pilot and production environments

Attributes:

* Self?motivated with a strong ownership and execution mindset
* Team player with excellent communication skills
* Hands?on, practical approach to experimental work

We are seeking a highly motivated and qualified Analytical Chemist for a temporary maternity leave replacement position with a strong passion for laboratory work. As part of our CMC team, you will play a central role in the chemical characterization of our products by developing and implementing analytical methods to identify and quantify both known and novel plant-derived compounds.
You will work closely with multidisciplinary teams - including QA/QC, Regulatory Affairs, Tech, and Clinical - to support drug development activities and regulatory submissions, including FDA approval of inhalation technology.
Key Responsibilities:
Operate, maintain, and troubleshoot analytical instruments such as GC/MS, UPLC, and Karl Fischer titrators.
Perform routine and non-routine chemical analyses.
Develop, optimize, and validate analytical methods.
Write and execute protocols related to method development and validation.
Contribute to the preparation of regulatory documentation for drug development submissions.
Support ongoing and future research and development initiatives.
Collaborate effectively with cross-functional teams to advance project goals.