- Mechanical product development using SOLIDWORKS and establishment of DHF for submittance to FDA & MDR.- Pressed for and led cross organizational projects to increase productivity and flexibility in manufacturing.- Identified redundancies and improved QMS procedures and work instructions to decrease production costs.- Developed processes with subcontractors to reduce non-conformities, substantially improving throughput.

- Directly managed the Engineering team & the department’s projects.- Operated in a medical device environment (ISO-13485, class II), and prepared the manufacturing aspects to FDA, MDD & MDR audits (ECOs, MRBs, Process Validations, IQ, OQ, PQ, etc.).- Full responsibility over all NPI activities & process development for the company’s entire portfolio as part of Transfer to Production (TTP), including establishment of complete DMR (BOM, PFMEA, SOPs, RCs, Flow Charts).- Full responsibility over Process Validations (IQ, OQ, PQ).- Established a preventative maintenance module for the company’s equipment and utilities. Implementation included eQMS paperless environment.- Packaging development for the company’s core technology (antibacterial nano particles). Project included design and development of mfg. process, under multiple conditions due to sensitivity of the product.

- Responsible for all process activities within the company (manufacturing, process safety, yield of 3 sites).- Pursue constantly after yield increase and lower OPEX:Developed customized data analysis and control tools to identify and monitor areas for yield improvement, process stability and to reduce machine fractures, resulting in $18k+/month savings and initiated projects totaling $3M, set generate a new source of income to the company.- Planning and execution of large scale projects, i.e. plant shutdowns, new equipment installations in tight schedules and ROI constraints:Saved $400k in downtime revenue loss in planned plant shutdown.- Conduct Root Cause Analysis (5-whys, fishbone, etc.)- NPI and assimilation of new process lines and updating existing processes' safety, stability, robustness.- Took part in global professional working groups developing new e-learning course to be used worldwide.- Operating in a medical standard environment: GMP, ISO-9001, MOC, HAZOP, CAPA, etc.

- Establishing R&D lab, devising and executing a scale-up plan, defining process stations and specifications for equipment, instruments and reactors while adhering to product quality and tight timelines.- Composing production protocol from a scaled-up POV with respect to safety considerations for each station in the production line.- Enhancing product ratio over cycle duration, waste etc. by spotting process parameters and adjusting the equipment accordingly.- Analysis and management of various QA tests. Building a database for trend analysis.- Procurement management, domestic and abroad, using Priority.

- Planning and assembling a pilot: equipment and instrument specification and arrangement, gas piping and solving problems that may happen while scaling-up.- Optimal planning of production cycles, manpower and optimization of yield / cost ratio.- Composing production protocol with respect to safety considerations for each station in the production line.- Design of Process Flow Diagrams (PFD's) and Pipe & Instruments Diagrams (P&ID's).- Ongoing management of the raw materials, maintenance cycles, waste treatment, workers, QA etc.

* Successful development of high capacity porous iron anode for flow cells.* Planning and executing experiments, reports and deducing conclusions for the next steps of the research.* Thorough and scrutinized analysis of previous data and identification of beneficial and limiting parameters.* Participation in multidisciplinary thinking groups for the improvement of other systems in the flow cell.* Participation in a course of "Optimal Design of Experiments" (DOE) and of the use of the JMP software.

* Chemical and mechanical development of fuel-cell based hydrogen on demand energy pack.* Taking extra curriculum courses in advanced electrochemistry for 2nd & 3rd degree.* Execution of business meetings with new investors and taking part in professional convention and exhibitions.* Using lab equipment such as FTIR, CIP, SEM, HPLC etc.

* Theoretical and Practical Training.* Diagnosing and troubleshooting software and hardware issues over the phone.

* Commanding and managing a company of 46 people.* Planning and revising outdated plans.* Experience with difficult employees.* Was responsible for the coordination of weekly maintenance checks for the battalions vehicles.