Scientist (Medical Industry)
Hoy
Trabajo visto
Descripción Del Trabajo
**Position Summary**
**Essential Duties and Responsibilities**
- Develops research plan, design experiments and outline research procedures to be followed
- Plans research schedule according to timetable and establishes daily or weekly routines necessary to meet the timetable.
- Develop projects from early development, product
Quality Engineer (Medical Industry)
Hoy
Trabajo visto
Descripción Del Trabajo
**Position Summary**
This position will assist with the ongoing monitoring, support, and continued improvement of QA Production processes and related activities and conduct periodic audits to ensure compliance and controls of the production processes.
**Essential Duties and Responsibilities**
- Implement statistical methods to inspect, test and evaluate the reliability of manufacturing and QA control processes, products, and production equipment.
- Determine quality improvement factors and improve QA Production SOPs and DHR forms.
- Implement and improve process controls to ensure on-time detection of potential product Quality issues and determination of appropriate follow up actions.
- Work with CAPA owners to complete investigation activities, determine root cause and implement appropriate Corrective and Preventive Action.
- Participates in the development of Validations (IQ, OQ, & PQ) for equipments, related with new products and/or manufacturing lines.
- Evaluate Non-Conformance records (NCMR’s) and support resolution of Quality issues.
**Requirements**:
- 2 years of experience (Medical Industry)
- Bachelor’s Degree in engineering or equivalent education
- Advanced english
- Current VISA
- IQ, OQ, PQ Validations
- Certified quality auditor, quality engineer or six sigma green belt (desirable)
- ISO 13485 and 21 CFR 820 (novice)
- GMP´s and GDP´s
- CAPA's/COR's/NCMR's & Complains
Tipo de puesto: Indefinido
Horario:
- Lunes a viernes
Pregunta(s) de postulación:
- Tiene experiência en auditorias internas y/o externas?
Educación:
- Licenciatura terminada (Deseable)
Idioma:
- Inglés (Deseable)
Smt Engineer (Medical Industry) Otay
Hoy
Trabajo visto
Descripción Del Trabajo
OBJETIVO: Asegura el buen funcionamiento de las máquinas SMT, sus procedimientos y formatos. FUNCIONES PRINCIPALES: 1. Mantenimiento Preventivo y correctivo en máquinas empastadoras, Montadoras (Pick and Place), Horno Reflujo, AOI, SPI. 2. Programación del equipo SMT 3. Mantiene la Integridad del Funcionamiento de las máquinas SMT 4. Asegurar que se complete el check list de arranque; así como la configuración del equipo. 5. Asegura que el Suministro de Materiales a las Tareas de Producción sea Oportuno y Preciso. 6. Realiza las Evaluaciones de Desempeño de sus Subordinados y crea los Planes de Desarrollo Pertinentes. 7. Desarrolla, Modifica y Mantiene los Procedimientos Estándares de Operación (SOP’s).
Experiência y requisitos
ESPECIFICACIONES DEL PUESTO: ESCOLARIDAD REQUERIDA: Profesional EXPERIENCIA REQUERIDA: Entre 2-3 Años en máquinas SMT (ASM, Juki, Panasonic, Yamaha, Fuji, Etc). NIVEL DE INGLÉS: Intermedio (Lectura y Conversación a nível Técnico). CONOCIMIENTO COMPUTACIONAL: Intermedio/Básico (Manejo de Office: Word, Excel, Power Point, Etc.) y Programas de Aplicación. UBICACION: OTAY HORARIO: DOMINGO A MIERCOLES DE 7:00AM A 7:00PM
Organización
North American Production Sharing de México, S.A. de C.V.
Correo de contacto
Giro
Maquiladora (Export.)
Actividad principal
Administración de maquiladoras.
Número de empleados
1000
**Área** Ingeniería
**Contrato** Permanente
**Turno** Diurno
**Jornada** Tiempo Completo
**Horario** DOMINGO A MIERCOLES DE 7:00AM A 7:00PM
**Estudios** Carrera Profesional
**Inglés **Hablado: 70%, Escrito: 70%
**Sexo** Indistinto
Smt Engineer (Medical Industry) Otay
Hoy
Trabajo visto
Descripción Del Trabajo
**FUNCIONES PRINCIPALES**:
1. Mantenimiento Preventivo y correctivo en máquinas empastadoras, Montadoras (Pick and Place), Horno Reflujo, AOI, SPI.
2. Programación del equipo SMT
3. Mantiene la Integridad del Funcionamiento de las máquinas SMT
4. Asegurar que se complete el check list de arranque; así como la configuración del equipo.
5. Asegura que el Suministro de Materiales a las Tareas de Producción sea Oportuno y Preciso.
6. Realiza las Evaluaciones de Desempeño de sus Subordinados y crea los Planes de Desarrollo Pertinentes.
7. Desarrolla, Modifica y Mantiene los Procedimientos Estándares de Operación (SOP’s).
**ESPECIFICACIONES DEL PUESTO**:
**REPORTA A**:Ingeniero de SMT Sr. / Gerente de SMT
**PUESTOS QUE LE PUEDEN REPORTAR DIRECTAMENTE**:Técnico de SMT.
**NÚMERO DE SUBORDINADOS QUE LE REPORTAN DIRECTAMENTE**:1 a 10 (Prom. 4).
**ESCOLARIDAD REQUERIDA**:Profesional
**EXPERIENCIA REQUERIDA**:Entre 2-3 Años en máquinas SMT (ASM, Juki, Panasonic, Yamaha, Fuji, Etc).
**NIVEL DE INGLÉS**:Intermedio (Lectura y Conversación a nível Técnico).
**CONOCIMIENTO COMPUTACIONAL: I**ntermedio/Básico (Manejo de Office: Word, Excel, Power Point, Etc.) y Programas de Aplicación.
UBICACION: OTAY
HORARIO: DOMINGO A MIERCOLES DE 7:00AM A 7:00PM
Tipo de puesto: Tiempo completo
Salario: $5,537.65 - $17,247.74 al mes
Horario:
- Diurno
Packaging Validation Engineer III (Medical Industry)
Publicado hace 11 días
Trabajo visto
Descripción Del Trabajo
BEPC Inc. provides Specialized Engineering Solutions and IT Project Management services to Fortune 500 companies in the Life Science and Technology industries. BEPC Mexico, a division of BEPC Incorporated, provides and manages consulting services for Automotive and Medical device companies throughout Mexico and around the globe.
We are looking for a Packaging Validation Engineer III to lead and implement changes in the packaging processes, for straight and square product lines, to validate equipment that makes up the process, including the sterile barrier system and the primary, secondary, and protective packaging. packaging. In this position, the day will include writing and executing packaging validation protocols, conducting change management assessments, creating, and executing engineering change orders, conducting engineering studies, and developing Designs of Experiments (DOE). In addition, lead studies, verification runs and the preparation of associated reports.
KEY RESPONSABILITIES:
- Lead and implement changes in the packaging components that make up the sterile barrier system, as well as protective packaging.
- Write/execute packaging validation protocols (IQ, OQ, TMV,) and their associated completion reports.
- Write/execute change management/change control assessments (e.g. validation, process, etc.).
- Create/execute engineering change orders.
- Create/execute engineering studies, verification runs and their corresponding completion reports.
BASIC QUALIFICATIONS:
- Bachelor's degree
- 2+ years of experience in the manufacturing industry.
- 3 years of experience in the Medical Device industry.
- Creation of IQ/OQ/PQ Protocols & Reports.
- ISO-13485 and ISO- CFR Part. 820
- Packaging Experience in medical industry
- Knowledge in packaging tests for lab equipment
- Advanced level of English , reading, writing and conversational (MUST).
- Willing to relocate to Santa Clara, California (MUST)
- TN Visa sponsorship available.
Packaging Validation Engineer III (Medical Industry)
Publicado hace 4 días
Trabajo visto
Descripción Del Trabajo
BEPC Inc. provides Specialized Engineering Solutions and IT Project Management services to Fortune 500 companies in the Life Science and Technology industries. BEPC Mexico, a division of BEPC Incorporated, provides and manages consulting services for Automotive and Medical device companies throughout Mexico and around the globe.
We are looking for a Packaging Validation Engineer III to lead and implement changes in the packaging processes, for straight and square product lines, to validate equipment that makes up the process, including the sterile barrier system and the primary, secondary, and protective packaging. packaging. In this position, the day will include writing and executing packaging validation protocols, conducting change management assessments, creating, and executing engineering change orders, conducting engineering studies, and developing Designs of Experiments (DOE). In addition, lead studies, verification runs and the preparation of associated reports.
KEY RESPONSABILITIES:
- Lead and implement changes in the packaging components that make up the sterile barrier system, as well as protective packaging.
- Write/execute packaging validation protocols (IQ, OQ, TMV,) and their associated completion reports.
- Write/execute change management/change control assessments (e.g. validation, process, etc.).
- Create/execute engineering change orders.
- Create/execute engineering studies, verification runs and their corresponding completion reports.
BASIC QUALIFICATIONS:
- Bachelor's degree
- 2+ years of experience in the manufacturing industry.
- 3 years of experience in the Medical Device industry.
- Creation of IQ/OQ/PQ Protocols & Reports.
- ISO-13485 and ISO- CFR Part. 820
- Packaging Experience in medical industry
- Knowledge in packaging tests for lab equipment
- Advanced level of English, reading, writing and conversational (MUST).
- Willing to relocate to Santa Clara, California (MUST)
- TN Visa sponsorship available.
Packaging Validation Engineer III (Medical Industry)
Hoy
Trabajo visto
Descripción Del Trabajo
BEPC Inc. provides Specialized Engineering Solutions and IT Project Management services to Fortune 500 companies in the Life Science and Technology industries. BEPC Mexico, a division of BEPC Incorporated, provides and manages consulting services for Automotive and Medical device companies throughout Mexico and around the globe.
We are looking for a Packaging Validation Engineer III to lead and implement changes in the packaging processes, for straight and square product lines, to validate equipment that makes up the process, including the sterile barrier system and the primary, secondary, and protective packaging. packaging. In this position, the day will include writing and executing packaging validation protocols, conducting change management assessments, creating, and executing engineering change orders, conducting engineering studies, and developing Designs of Experiments (DOE). In addition, lead studies, verification runs and the preparation of associated reports.
KEY RESPONSABILITIES:
- Lead and implement changes in the packaging components that make up the sterile barrier system, as well as protective packaging.
- Write/execute packaging validation protocols (IQ, OQ, TMV,) and their associated completion reports.
- Write/execute change management/change control assessments (e.g. validation, process, etc.).
- Create/execute engineering change orders.
- Create/execute engineering studies, verification runs and their corresponding completion reports.
BASIC QUALIFICATIONS:
- Bachelor's degree
- 2+ years of experience in the manufacturing industry.
- 3 years of experience in the Medical Device industry.
- Creation of IQ/OQ/PQ Protocols & Reports.
- ISO-13485 and ISO- CFR Part. 820
- Packaging Experience in medical industry
- Knowledge in packaging tests for lab equipment
- Advanced level of English , reading, writing and conversational (MUST).
- Willing to relocate to Santa Clara, California (MUST)
- TN Visa sponsorship available.
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Acerca de lo último Medtronic Empleos en Tijuana !
Financial Analyst (Medical Devices)
Hoy
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Descripción Del Trabajo
**RESPONSIBILITIES**:
- Produces ad hoc reporting & requests including but not limited to weekly sales report distribution, sales & financial monthly reporting
- Maintenance of business intelligence solution (Vena) including new
Buyer Direct (Medical Devices)
Hoy
Trabajo visto
Descripción Del Trabajo
Job Summary
To support our extraordinary teams who build great products and contribute to our growth, we’re looking to add a Buyer Direct located in Tijuana.
Reporting to the Purchasing Manager Direct, the Buyer Direct’s role involves:
What a typical day looks like:
- Reviews requisitions and MRP output.
- Confers with vendors to obtain product or service information such as price, availability, and delivery schedule.
- Determines method of procurement such as direct purchase.
- Orders, reschedules, and cancels material based on requisitions and MRP output.
- Maintains procurement records such as items or services purchased, costs, delivery, and inventories.
- Manages supplier to price, delivery and quality expectations and escalates when appropriate.
- Approves invoices for
Manufacturing Engineers (Medical Devices)
Hoy
Trabajo visto
Descripción Del Trabajo
**ACTIVITIES AND RESPONSIBILITIES**
- Establishes standards and policies for pollution control, installation, modification, quality control, testing, operating procedure, inspection, and maintenance of equipment and products.
- Conceptualize and institutes improvements to processes.
- Evaluates proposed improvements to processes and products based on analyses of regulatory requirements, product quality needs, ergonomics, safety, environmental and costs.
- Understands and utilizes the Quality System Requirements for design control and provides an appropriate engineering/technical assessment of data/documents supporting the design history file.
- Develops experimental design and statistical process control tools to assure process reliability, maintainability and safety.
- Evaluates fitness for use of materials, designs, processes, tests, and products.
- Design, execution, and analysis of experiments based on statistical techniques.
- Risk management development, troubleshooting and refinement of manufacturing processes and equipment.
- Performs and writes validations of product, processes and equipment in accordance with FDA, ISO and other applicable guidelines.
- Documents work via reports, technology notebooks, and design file entries.
- Develops procedures, trains other associates, and assists other technical associates.
- Hands-on involvement with all phases of his/her projects.
- Works effectively in team situations as well as independently.
- Performs other related duties as assigned or required based on education, knowledge, and previous experience.
**REQUIREMENTS**
- Requires a bachelor’s degree in Engineering.
- Experience a minimum of 4-5 year’s related experience.
- Experience In Medical Devices.
- Other Knowledge, Skills, Abilities or Certifications: Minimum 4years experience in the medical device or pharmaceutical industry.
- Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
- Ability to write routine reports and correspondence.
- Ability to speak effectively before groups of customers or employees of organization. Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.
- Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
**BUT ABOVE ALL**:
- Insatiable Curiosity
- Continuously Seeks to Improve
- Creativity and Innovation
- Problem Solving skills
- Good Communication & Leadership skills
- A Team Player
- Mathematical and Analytical Abilities Plus Logical Thinking
- Attention to Detail
- Embraces Change
- Optimistic