Medline

Quality Supervisor (supervisor Control de Calidad)

Medline

Jun. 10

Mexicali, Baja California

Organización

Medline

Giro

Manufacturera

Actividad principal

Global manufacturer and distributor of medical products with patient-centered solutions.

Número de empleados

2500

Dirección

Paseo S/N

Colonia o fraccionamiento

Parque Industrial El Desierto

Ciudad

Mexicali, Baja California

Descripción y detalle de las actividades

Coordinates all Quality control inspections in process and finished good to products, before and after sterilized (As applicable). Supports production departments to be in complaint with the QMS and company policies, promote development of personnel under his supervision. Coordinates and support all day to day activities taking into consideration production demand and priorities as well as QC inspector availability and level of training of the QC inspectors and leads. Coordinates inspection and testing to release regular or validation products as well as in non-conforming products. Provides support and helps to translate and interpreter product specifications contained on the different manufacturing and quality procedures. Notify and coordinates inspection to no conforming inventory components that affects the products acceptance. Support production areas to clarify existing doubts and provides guidance and responses related to quality control on products or manufacturing processes. Conducts daily checks audits with a Quality focus on the different Production áreas. Verifies and coordinates with QC leads the correct records filling as required by the applicable procedures during the inspection of the products/processes. Supervise QC inspectors and lead performance to assure quality objectives and company policies are met. Coordinates product release once all requirements indicated on specification or quality/manufacturing procedures have been met. Track, identify and segregates non-conforming product waiting for Disposition. Coordinate and trains QC inspector and leads on all applicable procedures. Evaluates performances of current and potential QC inspector’s candidates. Coordinates vacations and permits for its personnel. Coordinates Quality meetings and attendance. Implement Mysik ideas. Support personnel under his supervisión on Mysik

Experiencia y requisitos

Education: • Engineering degree (Industrial, electrical, related) • Bilingual 80%. Written and spoken Experience: • 2-3 years of experience as a QC supervisor on a similar industry. • FDA GMP knowledge. • ISO 13485 knowledge • Skill to manage big groups. Technical Skills: • Highly proficient on computer systems as MS Office, AS400, MRC. • Basic Statistics, sampling plan, AQL, Skip lot concept. • Tolerances and geometrics. • Measurement equipment. Interpersonal Skills: • Proactive person • Analytical • Outspoken • Responsible. • Effective communication • Leadership skills to work as teamwork • Work under pressure. • Quality oriented person

Número de vacantes

1

Área

Calidad

Contrato

Permanente

Turno

Mixto

Jornada

Tiempo Completo

Horario

3:00pm a 11:00 Pm Lunes a viernes

Estudios

Titulo Profesional

Inglés

Hablado: 80%, Escrito: 80%

Sexo

Indistinto