Senior Software Quality Engineer – Medical Device Compliance

A leading medical device company located in Mexicali, Baja California, is seeking a Software Quality Engineer to lead engineering activities ensuring compliance with regulatory standards. The role requires developing quality documentation, managing risk activities, and collaborating with global teams. Candidates should have a Bachelor's degree in a related...

Position SummaryThe Senior Packaging Engineer is responsible for supporting and driving packaging related projects through adherence to established quality system requirements, design control processes, good engineering, and documentation practices.The key responsibility of this position is to exercise medical device packaging subject matter expertise, sound...

**Descripción y detalle de las actividades**- The Quality Control Engineer (QCE) works with a team of dedicated individuals supporting manufacturing operations to assure quality of finished product and identify quality issues related to electrical, mechanical and software subsystems.The QCE evaluates product quality issues, performs root cause analysis,...

**Technimark** Empresa Líder a Nível Mundial de Inyección de Plásticos busca Candidatos para el puesto de**Ingeniero Calidad Senior **en su planta ubicada en**Mexicali, Baja California.**Reporta a:**Gerente de Calidad.**Supervisa a:** Inspectores de Calidad.****Experiência Requerida**:- 3 Años en Posición Similar.- 5 Años como supervisor de calidad,...

· Leadsoftware quality engineering activities across the full product lifecycle,ensuring compliance with ISO 13485, FDA QSRs, IEC 62304, ISO 14971, andrelevant cybersecurity and data-protection requirements. · Develop,review, and approve software quality documentation, including validation plans,protocols, reports, requirements traceability,...

· Leadsoftware quality engineering activities across the full product lifecycle,ensuring compliance with ISO 13485, FDA QSRs, IEC 62304, ISO 14971, andrelevant cybersecurity and data-protection requirements.· Develop,review, and approve software quality documentation, including validation plans,protocols, reports, requirements traceability,...

· Leadsoftware quality engineering activities across the full product lifecycle,ensuring compliance with ISO 13485, FDA QSRs, IEC 62304, ISO 14971, andrelevant cybersecurity and data-protection requirements.· Develop,review, and approve software quality documentation, including validation plans,protocols, reports, requirements traceability,...

A leading medical device company in Mexico is looking for a Manufacturing Engineer to enhance manufacturing processes through Lean tool implementation and continuous improvement. This role involves evaluating design reliability, ensuring compliance with quality systems, and maintaining production efficiency. The ideal candidate should have a bachelor’s...

A leading medical device company is seeking a Manufacturing Engineer to lead project management and technical solutions in their manufacturing processes. The role involves lean tool implementation and ensuring compliance with quality systems. Key qualifications include a Bachelor's degree in engineering and a minimum of four years experience in...

Descripción y detalle de las actividades The Sr. Quality Systems Engineer is the responsible in the development, implementation and follow up of the QMS (MDSAP, ISO13485 & FDA 21CFR Part 820) for MXC ensuring compliance to the applicable standards and regulations for the medical devices. Develop the internal audit program in MXC. Acts as Auditor Leader...