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Nextern

Designs and manufactures medical devices

IPQC Senior Engineer

Quality EngineeringConfirmed live in the last 24 hours
Full-timeHo Chi Minh City, VietnamNo salary listedIn-person

About the Job

Requirements

  • Ability to identify problems and develop and implement solutions.
  • Ability to make value-added decisions in a timely manner at all levels of the organization.
  • Ability to creatively develop effective responses and plans for people, problems, or issues.
  • Ability to communicate ideas, arguments, and solutions and work through conflict resolution internally and externally.
  • Ability to plan, implement, and communicate negotiation elements that create value while maintaining supplier relationships.
  • Consistently use good judgment and conduct work within corporate ethics guidelines.
  • Knowledge of ISO 9001:2015; knowledge of ISO 13485:2016 is preferable.
  • Understanding of process flow and quality control plans.
  • Knowledge of Failure Mode and Effects Analysis (FMEA).
  • Knowledge of process capability and control, and Minitab.
  • Understanding of drawing requirements and Acceptable Quality Limit (AQL) levels.
  • Bachelor’s degree or higher in an Engineering field or related technical degree; Mechanical or Electrical Engineering is preferred.
  • At least 5 years of quality experience.
  • Verbal and written communication skills in English.
  • Ability to speak clearly and persuasively in positive or negative situations, listen and clarify, respond to questions, present to groups, participate in meetings, write clearly and informatively, edit for spelling and grammar, adapt writing style to needs, present numerical data effectively, and read and interpret written information.
  • Knowledge of Microsoft Office.
  • Ability to read and interpret mechanical, electrical, and electro-mechanical drawings and models.

Responsibilities

  • Manage Corrective Action Preventive Action (CAPA) on the molding production line.
  • Evaluate process qualification and validation.
  • Manage the activities of quality inspectors.
  • Ensure production lines follow manufacturing procedures and production operators are trained to work on the lines.
  • Monitor process control, yield, and trends for other products.
  • Manage customer Return Material Authorizations (RMAs) to Nextern.
  • Perform failure analysis of returned products, including out-of-box and fielded products.
  • Manage non-conforming products on production lines.
  • Create documentation relevant to product specifications and requirements when assigned by the manager, including process flows, control plans, and inspection criteria.
  • Manage inspection of outgoing shipments.

Desired Qualifications

  • Experience with regulatory compliance submissions for Class I and Class II medical devices.
  • Extensive knowledge of FDA medical device regulations.

About the Company

Nextern

Designs and manufactures medical devices

Nextern designs and manufactures medical devices for equipment makers, with engineering and factory teams involved from early prototypes through production. Its work includes catheter-based instruments and electronic systems used in minimally invasive treatment and diagnostic procedures. Customers pay for development and contract manufacturing services, with project costs shaped by device complexity, materials and production scale. Its clinical markets include vascular and heart interventions and nerve stimulation, with services sold separately or as an integrated program. Founded in 2000 with industrial engineering roots, Nextern shifted to medical devices in 2016 and is headquartered in Maple Grove, Minnesota.

Company size
501-1,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Maple Grove, MN
Founded
2000

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