Product Engineer ; Medical Industry
Trabajo disponible en:
42976, Chihuahua, Hidalgo, México
Publicado en 2026-02-18
Empresa:
BEPC Inc. - Business Excellence Professional Consulting
Tiempo completo
puesto Publicado en 2026-02-18
Especializaciones laborales:
-
Ingeniería
Ingeniero de sistemas, Ingeniería de Calidad, Ingeniero de Manufactura
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 seeking a detail-oriented and technically proficient Validation Engineer I (Documentation and Configuration of products) to lead the obsolescence of products and parts within our systems. This role involves analyzing and modifying part numbers, BOMs, Routers, and affected Documents within the Product Lifecycle Management (PLM) and Enterprise Resource Planning (ERP) systems. The candidate will play a key role in ensuring the removal of parts no longer manufactured and continuous availability of components still in use, risk mitigation.
KEY RESPONSABILITIES:
Create and manage engineering changes such as COs, CPs and MVIs (Change Orders /Change Projects /Master validation Index) within the enterprise PLM (ADAPTIV) and ERP systems (JDE).
Experience in Product Lifecycle Management (PLM) programs.
Knowledge of Product Configuration: creation, modification, release, and obsolescence of bills of materials (BOM), part numbers, documents, specifications, work instructions, among others.
Work closely with design engineering, procurement, supply chain, and quality teams to assess impact and define resolution plans for obsolescence issues.
Liaise with manufacturers and distributors to verify part status, last time buys, and available replacements.
Generate and maintain obsolescence status reports including number of affected parts, product impact, risk assessment, and mitigation plans.
Ensure all changes and decisions are documented per company standards and meet regulatory and industry compliance requirements.
Complete all training in their area of responsibility within the assigned timeframe.
Follow all company safety policies and safety precautions in the work area.
QUALIFICATIONS:
Bachelor's degree in Engineering.
2 to 4 years of experience in the manufacturing industry and/or 2 to 3 years of experience in the medical industry.
Intermediate level of English (reading and writing) and intermediate English conversation skills.
Hands-on experience with PLM systems (e.g., Windchill, ADAPTIV, cPDM. Teamcenter, Agile) and ERP systems (e.g., SAP, Oracle).
Strong understanding of component lifecycle, BOM structures, and configuration management.
Experience with change management processes (ECR/ECO) (COs/CPs – Change Orders / Change Projects) MVIs (Master validation Index) and document control.
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