Empleos de Safety Stock, S. de R.L. de C.V en Baja California

A Supplier Quality Engineer is a professional who plans, develops, monitors, tests, maintains and improves as required, supplies, parts, components and/or raw materials for the assembly line, based on engineering and manufacturing specifications, monitoring materials, resolving as required quality concerns of products related to quality concerns of raw material and/or processes in industries such as manufacturing and/or services, and administrating Suppliers ensuring compliance with customer requirements, applicable standards and applicable regulations (21 CFR Part 820, EN ISO 13485, others applicable). Resolving quality concerns identifying opportunities for improvements, recommending solutions as result of a proper investigation, defining root cause (as applicable), and implementing required corrective and preventive actions to avoid occurrence and reoccurrence of identified opportunities. All described activities working along with Supplier, engineering, manufacturing, purchasing, warehouse, and any other company departments as required. Understand the term manufacturing as operations. Centerpiece S. de R.L. de C.V. (Manufacturing and Sterilization sites) applies as Manufacturer based on 21 CFR Part 820 Subpart A-General Provisions Section 820.3 Definitions (o) Manufacturer.

Duties:

 Secure supplies, parts, components and/or raw materials.

 Review engineering and/or manufacturing specifications

 Monitors materials for compliance.

 Contact vendors and liaise between product engineers, manufacturing personnel and suppliers to negotiate terms to secure required materials for the production floor.

 Conduct supplier quality control audits on a regular basis to ensure vendors and their supplies remain in compliance with company and federal manufacturing and production standards.

 Communicate with vendors regularly to address any concerns and foster an environment that facilitates continual improvement in working relationships.

house access by company and manufacturing management personnel.

 Determines quality improvement parameters by identifying statistical methods mainly relevant but not limited to suppliers processes as applicable.

 Establishes statistical confidence by identifying sample size and acceptable error and determining levels of confidence as applicable.

 Develops experiments by applying full and fractional factorial techniques if required and as applicable.

 Develops sampling plans by applying attribute, variable, and sequential sampling methods as applicable.

 Develops inspection plans for raw materials based on customer and/or engineering specifications.

 Maintains statistical process controls by applying demerit/unit, zone charting, x2 charts for distributions, p-charts, tendency charts, etc…, as applicable and as suitable to supplier and company processes.  Analyzes data by completing any of the tools to analyze data: hypothesis, normal distribution, process capability analysis tests, etc…, as applicable.

 Prepares reports by collecting, analyzing, and summarizing data; and making recommendations.

 Maintains professional and technical knowledge by attending educational workshops, reviewing professional publications, establishing personal networks and benchmarking state-of-the-art practices.

 Communicate, work and support internal and external customers inquires related to established QMS (Suppliers administration).

 Review, improve and approve as needed, qualifications and validations as required.

 Contributes to team effort by accomplishing related results as required.

 Ensures products adhere to company and industry quality standards administrating supplies, products, components and/or raw materials.

 Brainstorms ideas to create solutions for identified problems (supplier and/or company related).

 Performs all other duties and responsibilities that are reasonably assigned from time to time by the employer or its designated representative as needed.

Responsibilities:

 Duties count as responsibilities.

 Any responsibility agreed in any QMS documented processes.

 Performs all other responsibilities that are reasonably assigned from time to time by the employer or its designated representative as needed.

Authorities:

 Any authority agreed in any QMS documented processes.

 Performs all other authorities that are reasonably assigned from time to time by the employer or its designated representative as needed.

Tipo de puesto: Tiempo completo

Sueldo: $1,000.00 - $1,600.00 al día

Beneficios:

• Estacionamiento de la empresa
• Opción a contrato indefinido
• Seguro de gastos médicos
• Seguro de gastos médicos mayores
• Vacaciones adicionales o permisos con goce de sueldo
• Vales de despensa

Puede trasladarse/mudarse:

• 22706, Rosarito, B.C.: Trasladarse al trabajo sin problemas o planear mudarse antes de comenzar a trabajar (Obligatorio)

Experiencia:

• Industria medica: 1 año (Obligatorio)

Idioma:

• Inglés (Obligatorio)

Lugar de trabajo: Empleo presencial