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We are looking for an experienced Head of Process Engineering to lead our manufacturing processes during a critical growth phase.
This role includes end-to-end responsibility for process development, optimization, stabilization, and operational control, while building the process infrastructure needed to support production scale-up and long-term quality, consistency, and repeatability.
This is a highly Hands-on role, especially in the initial phase, with a strong focus on process improvement, troubleshooting, and operational stabilization. Full on-site presence in Caesarea is required due to the Hands-on nature of the role and the need for close involvement in process development, equipment oversight, production support, and cross-functional execution.
Key Responsibilities
Lead, develop, and optimize manufacturing processes across the company
Ensure process stability, repeatability, and scalability
Drive continuous improvement initiatives in early-stage production
Establish and implement process control methodologies
Identify and resolve process inefficiencies, deviations, and yield issues
Oversee machine operation, calibration, maintenance, and verification
Ensure proper documentation and compliance with equipment and operational procedures
Work closely with R&D on process development and transfer to production
Partner with QA to ensure process compliance, validation, and quality standards
Lead processes in an advanced manufacturing environment with a strong focus on precision, consistency, and control.

Job Description

Serve as the engineering and technical point of contact for the offshore facility

Collaborates with operations, maintenance, & construction personnel to identify, develop & implement offshore brownfield projects

Organizes and leads cross-functional teams to address complex issues or technical activities

Coordinates offshore construction and complex maintenance support vendors to ensure the highest level of safety, environmental, quality, & regulatory performance.

Verifies offshore equipment is installed and operates within company specifications, applicable regulations, industry codes, & Recognized and Generally Accepted Good Engineering Practices (RAGAGEP)

Develops and reviews relevant engineering and construction execution documents such as P&IDs, Construction Execution Workpacks, Risk Assessments, Piping Isometrics, Execution Schedules, Commissioning, Startup & Operations Procedures

Works in collaboration with stakeholders to clearly define project scope and objectives during the project development phase

Reviews EPC Contractor deliverables and ensure consistency with Design Specification for assigned facilities

Drives small project execution schedules within operating requirements and company business

objectives

Monitors project financial performance within planned company budget and overall business outcomes

Leads Facility system optimization efforts, defect elimination, and root cause analysis investigations

our company, a world leader in water treatment solutions is looking for a Project Engineer.
This is a unique opportunity to join a team with a significant impact on global water and environmental challenges.
Key Responsibilities:
Technical Lead for Tenders: Oversee the engineering aspects of bids and proposals, ensuring technical feasibility and accuracy.
Interface Management: Coordinate between internal engineering teams, external contractors, and suppliers to align technical specifications and costs.
Client & Stakeholder Communication: Serve as a technical point of contact for clients, addressing inquiries and presenting solutions.
Risk Assessment: Evaluate technical risks associated with new projects and propose mitigation strategies.
Location: Kadima (On-site).

We are looking for a Quality Engineer to join our Ink Plant.
This role combines responsibility for plant quality activities with ownership of the day-to-day laboratory operations. The position plays a critical role in supporting production continuity, ensuring product quality, strengthening process control, and leading investigations and continuous improvement initiatives.
The ideal candidate is analytical, structured, comfortable working under pressure, and motivated to grow within a dynamic manufacturing environment.
What should you have?
Quality Responsibility:
Lead deviation investigations and root cause analyses
Manage non-conformances and drive corrective and preventive actions (CAPA)
Strengthen in-process controls and quality monitoring systems
Support batch release decisions in alignment with plant procedures
Drive standardization, documentation improvements, and KPI tracking
Analyze quality trends and provide data-driven recommendations
Support audits and ensure compliance with internal quality standards
Laboratory Operations Responsibility:
Take responsibility for the day-to-day operation of the laboratory
Ensure timely testing and responsiveness to production needs
Perform hands-on laboratory testing and analysis as required
Maintain testing standards, documentation accuracy, and procedural compliance
Optimize laboratory workflows and improve operational efficiency
Work closely with Production, Engineering, Planning, and Supply Chain to ensure smooth plant operations.

We are looking for R&D Pharma Team Leader to be responsible for the professional and managerial leadership of R&D pharma team engaged in formulation and process development of drug products. The role includes building and executing work plans, managing timelines, providing scientific expertise of formulation and manufacturing process development, scale-up activities, transition of products from development to commercial manufacturing, leading process validations and technology transfers and supporting ongoing commercial manufacturing through deviation investigations and professional assessments, while continuously driving operational efficiency within the department.

Responsibilities:
Serve as a subject matter expert in formulation development, scale-up, and manufacturing processes.
Assign tasks, prioritize activities, and perform continuous follow-up on execution.
Ensure high-quality scientific and technical deliverables in compliance with GMP and regulatory standards.
Lead formulation and manufacturing process development in accordance with QbD methodology. Definition of QTPP, CQAs, CPPs, and Design Space.
Evaluation of experimental work, including scale-up activities from laboratory scale to Engineering to registration batches scale.
Lead and support process validation activities (Process Validation, PPQ). Review, assess, and approve validation protocols and reports.
Lead and participate in pharmaceutical technology transfer projects and transition of drug products from development status to commercial manufacturing, ensuring process robustness, regulatory readiness, and manufacturing continuity.
Collaborate with QA, Regulatory Affairs, Manufacturing, and Engineering to ensure successful product commercialization.
Identify risks, delays, and resource gaps, and lead mitigation actions.
Provide regular progress updates to management.
Actively participate in deviation investigations related to products in routine manufacturing and provide professional pharmaceutical opinions and assessments.
Perform root cause analysis and support definition and implementation of CAPAs.
Support change control activities related to products and processes.
Initiate and lead continuous improvement and efficiency initiatives within the department.
Implement pharmaceutical and regulatory best practices.

To apply, please send your application to our e-mail.