Product Release Associate

hace 2 semanas

Mexicali, México Intuitive A tiempo completo

**Company Description**: Descripción de la empresa

En Intuitive, estamos unidos detrás de nuestra misión: creemos que la atención mínimamente invasiva es la atención que mejora la vida. Mediante la inventiva y la tecnología inteligente, ampliamos el potencial de los médicos para curar sin limitaciones.

Como pioneros y líderes del mercado en cirugía robótica, nos esforzamos por fomentar un equipo inclusivo y diverso, comprometido con marcar la diferencia. Durante más de 25 años, hemos trabajado con hospitales y equipos de atención de todo el mundo para ayudar a resolver algunos de los desafíos más difíciles de la atención médica y avanzar en lo que es posible.

Intuitive se ha construido gracias a los esfuerzos de grandes personas de diversos orígenes. Creemos que las grandes ideas pueden provenir de cualquier lugar: nos esforzamos por fomentar una cultura inclusiva basada en la diversidad de pensamientos y en el respeto mutuo. Lideramos con inclusión y capacitamos a los miembros de nuestro equipo para que trabajen de la mejor manera y manifiesten su auténtica personalidad.

Las personas apasionadas que quieren marcar la diferencia impulsan nuestra cultura: los miembros de nuestro equipo se basan en la integridad, tienen una sólida capacidad para aprender, la energía para hacer las cosas, y aportan experiências diversas del mundo real para ayudarnos a pensar de nuevas maneras. Invertimos activamente en los miembros de nuestro equipo para apoyar su crecimiento a largo plazo y así poder continuar avanzando en nuestra misión y alcanzar su máximo potencial.

Únase a un equipo comprometido a dar grandes pasos hacia delante para una comunidad global de profesionales de atención médica y sus pacientes. Juntos, avancemos en el mundo de la atención mínimamente invasiva.

**Primary Function of Position**:
The Product Release Associate will work with multidisciplinary teams dedicated within Manufacturing, FQI, Planning and Engineering to assure compliance to of finished product quality system requirements, with the purpose to identify discrepancies related to traceability on the Device History Record, Rework of non-conforming products, ECO and Deviation implementation, Shipments of products to the sterilizer and help with the resolution of such discrepancies in order to authorize release of product to customers.

**Roles & Responsibilities**:

- Reviews and approves manufacturing Device History Records for all assembly levels, ensuring compliance with device master records and other Quality System requirements.
- Releases ISI products, including Instruments and Accessories for distribution according to the stablished procedures.
- Reviews and approves shipments of Single Use Devices to the sterilization process with the sterilizer contractor.
- Reviews, approves and releases sterile products from Intuitive or from a Contract Manufacturer.
- Documents non-conformances through the corresponding quality notification (NCR, VR, DN) on ISI electronic documentation system.
- Works collaboratively with internal and external customers to resolve non-conformances on a timely manner.
- Escalates areas of concern to the Quality Assurance department and direct management.
- Performs all work according to Quality standards as set by the Quality Assurance department and direct management.
- Performs all work according to production, planning and logistics schedule, including working overtime as required.
- Escalating to the Quality Assurance department and direct management all Quality issues that could impact patient safety, surgical efficacy or traceability.
- Compliance with company department and standard operation procedures.

Supports internal and external audits as required.

**Qualifications**:
**Skills, Experience, Education, & Training**:

- High School, Technical Diploma or Bachelor’s degree.
- 8 months to 1 year relevant experience in QA/QC role within a medical device company.
- Ability to read English, read and comprehend instructions, write short correspondences and memos, complete quality documentation in English and Spanish, effectively present information in one on one and small group situations involving employees, supervisors or engineers.
- Demonstrated understanding or aptitude to understand Medical Device QMS requirements and regulatory requirements.
- Demonstrated ability to be a quick learner and understand complex products and processes.
- Exceptional analytical, problem-solving, and root-cause analysis skills.
- Integrity: Accepting and adhering to high ethical, moral, and personal values in decisions, communications, actions and when dealing with others.
- Demonstrated ability to work independently and with mínimal supervision, multi-task, and handle tasks with competing priorities effectively.
- Very strong computer skills and experience with Windows operating system and Microsoft Office.
- Ability to travel domestically and internationally.
- Availability to work on

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