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Iso 14971 Jobs In Mexico - 26 Job Positions Available

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1 – 16 of 26 jobs
Fresenius Group jobs

Packaging Engineer 3 At Fresenius Medical Care, we are the global leader in kidney care, committed to improving the lives of patients with chronic kidney disease. Our mission is to deliver high-quality, innovative products, services, and

Fresenius Group  19 days ago
Johnson & Johnson jobs

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our

Johnson & Johnson  19 hours ago

Fresenius Medical Care Reynosa plant in Mexico seeks a Regulatory Affairs Expert to manage global documentation, registrations, and regulatory compliance across product lifecycles. You will lead regulatory aspects of changes and provide guidance on standards and

CH01 CHE Fresenius Medical Care (Schweiz) AG  18 days ago

Johnson & Johnson in Ciudad Juárez, Mexico seeks a Senior Quality Life Cycle Engineer to lead quality engineering across the product life cycle, emphasizing reliability, risk management, statistics, and design control from development to manufacturing. You

Johnson And Johnson  18 days ago
PQE Group jobs

We are seeking experienced Design Controls and Design History File (DHF) Remediation Specialists to support medical device manufacturers with quality system and product lifecycle compliance initiatives. The successful candidate will serve as a subject matter expert

PQE Group  16 days ago

TAXAN SWE in San Luis Potosí is seeking a Mechanical Engineer to validate processes and ensure products meet customer requirements across assemblies and components. You will coordinate risk management studies under ISO 14971, manage change control, supervise design

TAXAN SWE  7 days ago
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Sr. Quality Engineer Top 5 Key Responsibilities Represent Quality in cross-functional projects, ensuring compliance with regulatory and internal quality standards. Support process verification and validation activities (IQ/OQ/PQ), including documentation and reporting. Collaborate in the development and

Oferta Confidencial  4 hours ago
Celestica jobs

Summary Responsible for HT quality plan, culture initiatives and monitoring of objectives and KPIs. Own the global QMS training strategy; develop minimal requirements for training, onboarding and refresher training for all HT employees, assign, and track

Celestica  3 days ago

Experienced and skilled degreedengineer that provides solutions to a variety of technical problems of moderatescope and complexity. They typically will connect to tasks or to the completion of milestones of projects. Sr. Quality Engineer can lead

Quasar Medical Tecate S.A. De C.V.  4 hours ago

Mechanical Engineer San Luis Potosí | Manufacturing Industry Full-time | On-site Key Responsibilities: Validation: Validate processes and products to ensure compliance with customer requirements for assembled products and the processes used to manufacture components and assemblies.

TAXAN SWE  3 days ago
Celestica Inc. jobs

10 - Manager, Global QMS Date: Jul 10, 2026 Location: Monterrey, NLE, MX General Overview Functional Area: Operations (OPS) Career Stream: Quality (QUA) Role: Manager 2 (MG2) Job Title: Quality QMS Manager Job Code: MG2-OPS-QUA Job

Celestica Inc.  1 day ago

El Ingeniero de Proyectos es responsable de liderar proyectos de ingeniería de principio a fin, asegurando el cumplimiento de los objetivos de calidad, costo y tiempo dentro de un entorno altamente regulado. Este rol coordina actividades

Wellspect HealthCare  3 days ago
Fisher & Paykel Healthcare jobs

Join a team of good people doing good work with intent. People like you, who care to make a difference. About The Opportunity Our strong focus on research and development creates a regular flow of new

Fisher & Paykel Healthcare  3 days ago

Oferta confidencial is seeking a Sr. Quality Engineer in Tijuana, Mexico to lead quality initiatives, coordinate cross-functional projects, and ensure compliance with medical device standards. The role focuses on process validation, documentation, and continuous improvement with

Oferta Confidencial  3 days ago
Outset Medical, Inc. jobs

The Senior Supplier Quality Engineer (SQE) plays a critical role in maintaining and continuously improving the quality of materials and components procured by the business. This position oversees supplier performance, provides regular reports to management to

Outset Medical, Inc.  3 days ago
Outset Medical jobs

Position Overview The Senior Software Quality Engineer is responsible for performing design assurance activities for new introductions and sustaining of medical device software, with the purpose of supporting the Software R&D, Test and Manufacturing departments. The

Outset Medical  2 days ago

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