Kiryat-Ono, ISR
1 day ago
Senior Engineer
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Supply Chain Engineering **Job Sub** **Function:** Repair & Maintenance Engineering **Job Category:** Scientific/Technology **All Job Posting Locations:** Kiryat-Ono, Tel Aviv District, Israel **Job Description:** **About Surgery** Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of surgery? Ready to join a team that’s reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the world’s most prevalent conditions such as obesity, cardiovascular disease and cancer. Patients are waiting. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech **We are looking for the best talent for** **Senior Utilities and Process Engineer** **to join our Engineering department in our Tel-Hashomer site.** **In this role you Will:** + Apply extensive and diversified knowledge of engineering and validation principles and practices in a broad range of assignments and related fields. + Be responsible for the performance of all issues related to engineering and validation department's activities. + Make decision regarding engineering and validation problems and methods, problem solving, and all other issues related to engineering and validation activities. **Duties & Responsibilities** + Reviews and analyzes complex task statements, standards, specifications, engineering drawings and other documentation to determine engineering requirements + Uses engineering and/or validation judgment in anticipating and solving unprecedented engineering and/or validation problems + Conceives and plans investigations of broad areas of considerable novelty and importance for which engineering and/or validation precedents are lacking in areas critical to the overall engineering and validation program + Analyzes customer technical requirements and recommends solutions beneficial to the customer and to the company + Responsible for assuring that the generation, release, and maintenance of documentation is in accordance with all requirements. + Designs complex mechanical, electronic and electrical assemblies and systems + Provides technical expertise and assistance to assigned engineers and technicians. + Analyzes test data for accuracy and consistency. Inspect, certify and evaluate onsite operational systems and establishes test plans + Determines appropriate test criteria and procedures and analyzes data comparing against specified and computed values, making changes and improvements where needed + Plans and conducts work requiring judgment in the independent evaluation, selection and substantial adaptation and modification. + Contributes extensively to engineering standards development balancing corporate and customer needs. Performs complex research of new technology for potential corporate application + Responsible to follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition + Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures **Experience and Education** + Engineering University/Bachelor's Degree or Equivalent + Generally, requires (6-8) years related experience + Specific types of experience that may be required for this position: + Experience in the pharmaceutical industry + Experience in project management and project management methodologies + Experience in data analyzing methods, assessing processes, taking measurements and interpreting data + Experience in budget management and expenses planning + Ability to work cooperatively with coworkers + Experience in the pharmaceuticals industry regulation + Ability to perform duties in accordance with policies and procedures + Ability to communicate effectively with a diverse clientele base + Demonstrated knowledge of manufacturing principles, practices, and procedures + Demonstrated knowledge of commissioning and de- commissioning documentation writing and performance + Demonstrated knowledge of maintenance, operating instructions documentation writing + Demonstrated skills for Developing, configuring and optimizing industrial processes from inception through to start up and certification + Maintain reliable and safe manufacturing systems while improving production rates, efficiencies, yields, costs and changeovers. + Develop innovative solutions. + Improve process capability and production volume while maintaining and improving quality standards.
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