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Parque Industrial Thomas Alva Edison (Rosarito)

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Manufacturing Engineer (Medical)

Summary: The Manufacturing Engineer applies knowledge of continuous improvement to enhance manufacturing quality, reliability, and cost-effectiveness. May design, or work with designers, to refine product designs, to increase manufacturability, and decrease costs.

Essential Duties and Responsibilities:

  • Applies lean manufacturing techniques to reduce manufacturing waste.
  • Conducts time studies and adjusts production standards as required.
  • Provides direct production area support and identifies potential process improvements, efficiencies and safety issues. Continually monitors scrap rates and initiates projects to reduce scrap cost in manufacturing.
  • Works with team leaders and production management to reviews shop order variances (material and labor) and initiates projects to eliminate variances and improve actual cost performance.
  • Trains work cell team members in continuous improvement working with team leaders and production supervision to create a culture of continuous improvement.
  • Verifies and understands work Instructions to communicate the proper set-up and operation of manufacturing processes to produce products which meet customer requirements.
  • Trains production team members in the development and use of visual production tools to promote improvements to product quality and production efficiency,
  • Collects and utilizes data to make data driven decisions.
  • Provides reports summarizing problem solving and corrective action efforts to production teams and customers as required.
  • Ability to assist in the design, install and troubleshoot basic manufacturing equipment such as jigs, fixtures and gages. Ability to execute IQ/OQ/PQ activities.
  • Utilizes engineering methodologies to determine root cause of failures using statistical methods and recommends changes in designs, tolerances, or processing methods.
  • Submits capital projects for approval, as required.
  • Prepares reports summarizing information or trends related to manufacturing performance.
  • Trains production personnel in new or existing methodology.
  • Supports new product transfer into production, working with company’s Transfer teams.

Qualification Requirements:

  • BS degree in engineering or relevant discipline; plus 3+ years in manufacturing engineering preferred, or an equivalent combination of education and experience.
  • Must have knowledge of lean manufacturing and other continuous improvement manufacturing methodologies. Experience with GD&T, CAD, Minitab, MS Project strongly desired.
  • Experience in Medical Device manufacturing and regulatory requirements is highly preferred.
  • Experience with regulated quality systems like ISO-9001, ISO-13485 and FDA regulations or industry equivalent.
  • Knowledgeable/Skilled in applying statistical analysis to develop and control processes in a manufacturing environment.
  • Manufacturing experience must include heavy emphasis on assembly operations, tooling evaluation, validations and cost savings through process improvement.

Other Job-Specific Requirements:

  • Bilingual in English / Spanish (Fluent).
  • Excellent interpersonal and communication skills (both verbal and written).
  • Strong people management and development skills.
  • Strong listening skills.
  • Occasional travel to the United States may be required; Passport and Visa required.
Reference :
UFP
Contract :
Permanente
Job(s) available(s) :
2
Experience :
3~8 Años
Studies level :
Carrera Profesional
Working place :
TIJUANA
Creation date :
10/18/2021
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Co-Production International Mexico Manufacturing Service Provider

mexico icoMexico Corporate Office
Phone: +1855.480.0837 / +52(664)454-3330
Blvd. Corredor Tijuana-Rosarito 2000
15202 Int. Mt8, Zona Cerril General
Tijuana, BC 22330, Mexico
reclutamiento@co-production.net

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