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 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
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
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
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
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
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
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
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
Do you have a passion for helping launch and manufacture innovative medical and drug delivery devices that can help improve lives? We are growing and looking for a Design Transfer Engineer to help create innovative solutions
En pocas palabras Posición: Medical Device Development Team Leader Localización: Azuqueca de Henares (Presencial) Experiencia: al menos 5 años en el desempeño de las funciones descritas ¿Quieres saber más? INSUD PHARMA opera en toda la cadena
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
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.
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
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
Insulet started in 2000 with an idea and a mission to enable our customers to enjoy simplicity, freedom and healthier lives through the use of our Omnipod® product platform. In the last two decades we have
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