Explore 6 process engineering jobs from 2 hiring companies in Encinal, TX, US. Filter by remote, salary, experience, and company, then open any listing to apply.

process-engineering

Process Engineering

Laredo

Cactus

Cotulla

Carrizo Springs

Rio Bravo

Dilley

El Cenizo

Freer

Gardendale

Asherton

Larga Vista

Big Wells

Ranchos Penitas West Colonia

Ranchos Penitas West

Pueblo Nuevo Colonia

Pueblo Nuevo

Carrizo Hill

Process Engineering Jobs

Medline

Baker Hughes

Onsite

Job DescriptionObjetivo General:Administrar al departamento de Ingeniería de Procesos, brindar estrategias para el cumplimiento de métricas y objetivos para la fabricación de productos asegurando que cumplan con las especificaciones de calidad de la manera eficiente.Responsabilidades:<ul><li>Responsable de Administrar, Guiar y Desarrollar al departamento de ingeniería de Procesos. </li><li>Generar Estrategias para el cumplimiento de los métricos. </li><li>Desarrollar y optimizar los procesos en la cadena de valor, así como actualizar o implementar sistemas y documentación relacionada para el control y mejora de los mismos. </li><li>Asegurar que los proyectos e ideas de mejora de calidad, costo, eficiencia, administración y seguridad del grupo de Ingeniería de Procesos terminen de forma exitosa y en tiempo. </li><li>Monitorear y controlar los resultados de costo, eficiencia y productividad, y establecer planes de acción cuando sea necesario, además de elaborar presupuestos y proyecciones en estos aspectos. </li><li>Investigar, evaluar e implementar nuevas tecnologías para los procesos. </li><li>Utilizar metodologías como MKOS, Lean Manufacturing, Solución de Problemas y Calidad, Core Tools, 6 Sigma y Metodología de MKOS en la ejecución de actividades y proyectos del área y del personal a cargo. </li><li>Contribuir en eventos Kaizen, programas de MKOS, CAPAS y órdenes de C-hold según se requiera. </li><li>Garantizar que las operaciones se realicen de acuerdo a los estándares de calidad para evitar OFIs y NCs internas y externas.</li></ul>Experiencia:<ul><li>Bilingüe (inglés – español) 85%(B2). </li><li>Experiencia mínima de 3 años industria Medica/Quirúrgica en roles directamente relacionados con procesos de Manufactura o Logística de Almacén.</li><li>Conocimiento y experiencia en Automatización, incluyendo control, neumática, mecánica, hidráulica, eléctrica, programación e integración.</li><li>Familiaridad con procesos de moldeo, extrusión, FFS (Form, Fill, Seal), procesos de almacén y automatización. </li><li>Dominio de Competencia y habilidad de implementación en Lean Manufacturing, Herramientas de Solución de Problemas y Calidad, Core Tools, 6 Sigma, Metodología de MKOS. </li><li>Manejo de Minitab, AutoCAD, AS400, M-Power, Pack Draw, Macros, Adobe, Microsoft office (Project, Excel, Word, Power Point, Outlook) (avanzado). </li><li>Capacidad para interpretar y analizar datos para la toma de decisiones. </li><li>Conocimiento en del estándar ISO-13485 Medical Devices Quality Management Systems.</li><li>Conocimiento básico de programación de sistemas computacionales. </li><li>Experiencia como auditor interno de calidad (deseable)</li></ul>Competencias /softskills <ul><li>Trabajo en equipo, facilidad de interpretación de datos, determinado, proactivo, orientado a resultados, sentido de urgencia, liderazgo, orientado al personal, habilidades de negociación. </li><li>Toma de decisiones que lleven a resultados positivos de acuerdo a análisis.</li><li>Habilidad para administrar diferentes recursos según sus capacidades individuales, así como el desarrollo y retención de estos.</li><li>Disponibilidad entre turnos. Responsable y profesional en todo momento. </li></ul>Formación académica <ul><li>Ingeniero en Procesos y Operaciones Industriales, Mecatrónica o Carrera. equivalente relacionadas a proceso industriales o automatización. </li><li>Certificado en Lean Six Sigma Green Belt PMBOK.</li><li>Maestría Relacionada en Procesos Industriales (Deseable). </li><li>Certificación Black Belt (Deseable).</li></ul>Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, disability/handicap status or any other legally protected characteristic.

Process Engineering Assistant Manager

Bilingual (English/Spanish); 3+ years in medical/ surgical manufacturing or warehouse logistics; automation experience; Lean Six Sigma; strong data analysis; proficient with Minitab, AutoCAD, AS400, M-Power, Pack Draw; ISO-13485 knowledge; internal quality auditor experience preferred.

Job Description<h1>CORE JOB RESPONSIBILITIES:</h1><ul><li>Develop, re-design, and essentially own change management of process changes. This may include changes to formulations, methods and controls to meet quality standards within guidelines and standards.</li><li>Identify complex technical issues or operational bottlenecks, determine root causes, and recommend and implement improvements, modifications or additions to document work using proven statistical methods. This may be with overall process or with product related issues.</li><li>Review step-change or change requirements for compatibility with processing methods to determine costs and schedules in addition to planning, and directing the installation, testing, operation, maintenance and repair of manufacturing and facilities equipment</li><li>Integrate equipment and material capabilities to meet process module target specifications and technology target specifications.</li><li>Partner with team of engineers, site leadership and/or continuous improvement team to provide support in process adherence endeavors or more likely to change process to accommodate identified opportunities.</li><li>Support long-term continuous improvement to implement solutions to various projects. Analysis may include fishbone, 5 why, DMAIC, RCA, work measurement (time study) and statistical analysis.   </li><li>Develop sequence of operations, estimate time requirements for each and prepare operation sheets; with an eye to deploy. This includes support of the labor management system (LMS) and warehouse management system (WMS) for local sites.</li><li>Partner with engineering team and local leadership on the development of SOPs for learning and development to build documentation on standards to facilitate team member training</li></ul><h1>BASIC QUALIFICATIONS: </h1>Education Bachelor’s degree in related Engineering disciplineRelevant Work ExperienceAt least 3 years of experience in related roleExperience with equipment troubleshooting and problem solving.<h1></h1><h1>PREFERRED QUALIFICATIONS:  </h1>Certification / LicensureLean Training, Six Sigma Training, Tableau or other statistical analysis packagesMedline Industries, LP is an equal opportunity employer. Medline evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, disability/handicap status or any other legally protected characteristic.

Engineer Process

Process Engineer

Bachelor's degree in engineering; minimum 3 years' related experience; skilled in equipment troubleshooting and problem solving; Lean and Six Sigma training; experience with Tableau or similar statistical analysis tools.

Job DescriptionObjetivo General:Administrar al departamento de Ingeniería de Procesos, brindar estrategias para el cumplimiento de métricas y objetivos para la fabricación de productos asegurando que cumplan con las especificaciones de calidad de la manera eficiente. Responsabilidades / Funciones:Responsable de Administrar, Guiar y Desarrollar al departamento de ingeniería de Procesos.Generar Estrategias para el cumplimiento de los métricos.Desarrollar y optimizar los procesos en la cadena de valor, así como actualizar o implementar sistemas y documentación relacionada para el control y mejora de los mismos.Asegurar que los proyectos e ideas de mejora de calidad, costo, eficiencia, administración y seguridad del grupo de Ingeniería de Procesos terminen de forma exitosa y en tiempo.Monitorear y controlar los resultados de costo, eficiencia y productividad, y establecer planes de acción cuando sea necesario, además de elaborar presupuestos y proyecciones en estos aspectos.Investigar, evaluar e implementar nuevas tecnologías para los procesos.Utilizar metodologías como MKOS, Lean Manufacturing, Solución de Problemas y Calidad, Core Tools, 6 Sigma y Metodología de MKOS en la ejecución de actividades y proyectos del área y del personal a cargo.Contribuir en eventos Kaizen, programas de MKOS, CAPAS y órdenes de C-hold según se requiera. Garantizar que las operaciones se realicen de acuerdo a los estándares de calidad para evitar OFIs y NCs internas y externas.Experiencia/ conocimientos técnicosBilingüe (inglés – español) 85%(B2).Experiencia mínima de 3 años industria Medica/Quirúrgica en roles directamente relacionados con procesos de Manufactura o Logística de Almacén.Conocimiento y experiencia en Automatización, incluyendo control, neumática, mecánica, hidráulica, eléctrica, programación e integración.Familiaridad con procesos de moldeo, extrusión, FFS (Form, Fill, Seal), procesos de almacén y automatización.Dominio de Competencia y habilidad de implementación en Lean Manufacturing, Herramientas de Solución de Problemas y Calidad, Core Tools, 6 Sigma, Metodología de MKOS.Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, disability/handicap status or any other legally protected characteristic.

Superintendente Ingenieria Procesos

Process Engineering Superintendent

Bilingual Spanish-English; 3+ years in medical/manufacturing or warehouse logistics; automation knowledge; Lean, Six Sigma, MKOS; process improvement.

Job DescriptionGeneral Objective:Ensure product processing, regulatory requirements, and equipment requirements are met in accordance with specifications including calibrations, internal, customer and regulatory audits, validations, record keeping and reporting for routine sterilization.Responsabilities:<ul><li>Review sterilization records and all related documentation for completeness, accuracy, and to ensure they meet validated parameters prior to releasing product for distribution.  </li><li>Verification and transmittal of various biological and product samples for customers’ routine sterilization and validation loads.</li><li>Assist in validation product load set up including placement of samples and sensors within product cases and distributed throughout a load. Configure samples and product cases onto pallets according to validation study instructions and retrieve samples at designated times after processing for transmittal to laboratory.  </li><li>Assist in preparation of protocols and reports for customer sterilization validations.  Review test results, run records, analyze temperature and humidity data to ensure they meet the acceptance criteria of the protocol.</li><li>Configure, set-up, and download sensors used for various customer validation and equipment qualification studies. Review and ensure sensors meet calibration specifications prior to and after studies as defined in Medline procedures or customer protocols.</li><li>Maintain sterilization related document historical files by physically sorting/boxing and electronically scanning to ensure access throughout defined retention period.</li><li>Review various facility processing and maintenance documentation including process logs, equipment maintenance, equipment qualifications, and calibration records for completeness and acceptability. </li><li>Interact with individuals from different disciplines (Production, Maintenance, and Customers) to plan, execute and complete EO validation activities according to time sensitive schedules.</li><li>Maintain inventory and review usage logs for customer supplied biological indicators used for routine sterilization process monitoring and communicate with customers on needs.</li></ul>KNOWLEDGE/EXPERIENCE       <ul><li>Intermediate level skill in Microsoft Excel. And Word        </li><li>Intermediate level skill in Microsoft Word         </li><li>1&#43; Years working in FDA/ISO 13485 regulated environment---Desirable        </li><li>1&#43; Years working in Medical Device manufacturing--Desirable        </li><li>-Must be willing to work safely in environments where hazardous materials may be present.        </li></ul>SKILLS         <ul><li>Effective communication   </li><li>Proactive   </li><li>Able to manage multiple projects   </li><li>Availability   </li><li>Sense of Urgency   </li><li>English 80%       </li></ul>EDUCATION<ul><li>Bachelor Degree    </li></ul>Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, disability/handicap status or any other legally protected characteristic.

Engineer Sterilization

Sterilization processing, QA/document control, FDA/ISO 13485 environment; strong Excel/Word; English 80%; Bachelor's degree; 1+ years in medical device setting.

Bakerhughes

<div>Would you like to ensure high-quality and safe logistics for our chemical operations?</div><div><div><div><div><div><div><div><div><div>Do you enjoy working as a team to deliver exceptional customer serviceOur Upstream Chemical Team uses technology consisting of chemistry, knowledge expertise, intelligent property. Correct application methods and monitoring to improve the process treatment applications at refinery and industrial plants, providing value to our clients. Our team has an essential role in ensuring the safe and efficient delivery of our products to our customer location.Deliver a flawless service to our customersYou will be responsible for:<ul><li>Under supervisor direction, provides support to measure product performance of existing programs.</li><li>Conducting and reporting product field test results.</li><li>Monitoring product tests and operating parameters and records and/or communicates results to supervisor.</li><li>Conducting maintenance on equipment as directed.</li><li>Completing product inventory management practices, which may include inventory reporting, ordering, and delivery.</li><li>Conducting all business activities in accordance with Baker Hughes HSE policies, Legal Compliance requirements and Baker Hughes Core Values.  </li></ul>Fuel your passionTo be successful in this role you will:<ul><li>General knowledge of basic processes and business principles.</li><li>Knowledge of chemistry, materials, process flows and petroleum engineering concepts. Ability to work and communicate well with others.</li><li>Qualifications Two-year Technical College Degree or equivalent preferred.</li><li>Successfully completes required training through participation in the LEAD–Field Specialist Development Program, which includes in-depth training activities focused on HS&amp;E, compliance, oilfield industry and basic product line products and services.</li></ul> Work in a way that works for youWe recognize that everyone is different and that the way in which people want to work and deliver at their best is different for everyone too. In this role, we can offer the following flexible working patterns:<ul><li>This role will be Monday-Friday with occasional overtime</li><li>Flexible to work weekends if need be.</li></ul> Working with usOur people are at the heart of what we do at Baker Hughes. We know we are better when all of our people are developed, engaged and able to bring their whole authentic selves to work. We invest in the health and well-being of our workforce, train and reward talent and develop leaders at all levels to bring out the best in each other.Working for youOur inventions have revolutionized energy for over a century. But to keep going forward tomorrow, we know we have to push the boundaries today. We prioritize rewarding those who embrace change with a package that reflects how much we value their input.  Join us, and you can expect:<ul><li>Contemporary work-life balance policies and wellbeing activities</li><li>Comprehensive private medical care options</li><li>Safety net of life insurance and disability programs</li><li>Tailored financial programs</li><li>Additional elected or voluntary benefits</li></ul></div></div></div></div></div></div></div></div></div><h3></h3><h3></h3>You will be eligible to participate in Company-sponsored benefit programs, including health &amp; welfare programs and the Thrift Plan (401k). You will have a choice of coverage options that best suit your needs. Coverage options and contribution amounts are related to your benefit elections, base salary level, and specific requirements of each of these plans. This position is eligible for our comprehensive and competitive benefits package, which can be found <a href="https://nam12.safelinks.protection.outlook.com/?url&#61;https%3A%2F%2Fwww.bakerhughesbenefits.com%2Fguide&amp;data&#61;05%7C02%7CSHRIJA.NEEMA%40bakerhughes.com%7Cd395b1802c834603fa8e08dc43a37ca4%7Cd584a4b7b1f24714a578fd4d43c146a6%7C0%7C0%7C638459616712836108%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C0%7C%7C%7C&amp;sdata&#61;T%2B63fCdcAYmaPH0GXOxEUyHaQaCDCUFc0ILPtVAtowk%3D&amp;reserved&#61;0" target="_blank">here</a>, and is further eligible for additional forms of compensation such as bonuses subject to the terms of the applicable benefit plans or policies.  The Baker Hughes internal title for this role is: Service Rep Gen Chemical

Service Rep GEN Chemical

Two-year technical college degree or equivalent preferred; knowledge of chemistry, materials, process flows and petroleum engineering concepts; ability to work with others; LEAD–Field Specialist Development Program training.

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