Quality Engineer

at  LUXWALL INC

Litchfield, Michigan, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate26 Jul, 2024USD 90000 Annual30 Apr, 20245 year(s) or aboveLean Manufacturing,Six Sigma,Iso Standards,Teamwork,Analytical SkillsNoNo
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Description:

QUALITY SYSTEMS ENGINEER

LuxWall is focused on the product development, scaling and commercializing of innovative glass products and solutions for the built environment. LuxWall’s transparent insulation technology, Enthermal Glass, provides a step change in energy performance by significantly reducing convective, conductive, and radiative heat gain and heat loss in buildings. Acting as a transparent thermos bottle for building, LuxWall has the potential to reduce global carbon emissions by more than 0.5 gigaton per year with mass adoption. Enthermal glass will forever change the way buildings are designed and constructed for the future sustainability of our plant.
A Quality Systems Engineer is a professional who ensures that all products within a company meet consistent standards. They develop and implement quality control tests to ensure the company’s result is what it should be, inspecting at various production stages and writing reports on their findings to act where needed.

POSITION REQUIREMENTS

  • Bachelor’s Degree in business, engineering or another technical field required, or High School diploma or equivalent of 5-7 years relevant manufacturing Quality experience required.
  • IATF Internal Auditor certification is required.
  • IATF Lead Auditor preferred.
  • Working knowledge of Lean Manufacturing, 5-S, Total Quality Concepts, and Six Sigma.
  • Possess a robust understanding of the IATF and ISO standards and their implementation.
  • Hands-on approach to problem solving and analysis.
  • Excellent Data Analytical Skills.
  • Ability and willingness to uphold the Company Values of Safety, Customer Focused, Teamwork, Excellence and Trust.
    All applicants must complete and pass a drug screening and background check. LuxWall’s process is a 10-panel drug screen which includes marijuana.
    Interested applicants please copy and paste this link into your browser:
    https://form.jotform.com/231704430398152
    Job Type: Full-time
    Pay: $90,000.00 - $130,000.00 per year
    Work Location: In perso

How To Apply:

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Responsibilities:

  • Maintain plant compliance to standards as well as customer defined quality systems and requirements.
  • Oversee the evaluation of process audits and finished product inspections for quality and reliability.
  • In conjunction with Corporate Quality, develop internal quality control standards for the plant.
  • Ensure quality systems and procedures are maintained and effectively used by all associates.
  • Ensure effective quality training for all team members.
  • Communicate significant quality issues throughout all levels of the Company.
  • Develop and maintain a partnership-style relationship with customers and suppliers.
  • Work closely with other managers to address the day-to-day problems and improve product/process quality.
  • Prepare department budgets and forecasting, as necessary.
  • Ensure quality policies, procedures and initiatives are compliant with Company standards.
  • Prepare and distribute daily, weekly, monthly/annual reports depicting the Key Performance Indicators and progress toward targets.
  • Ensure all government-required testing, reporting and recordkeeping is completed as required.
  • Provide guidance and direction to subordinates, including setting performance standards and monitoring performance.
  • Understand customer needs and requirements to develop effective quality control processes.
  • Devise and review specifications for products or processes.
  • Set requirements for raw material or intermediate products for suppliers and monitor their compliance.
  • Ensure adherence to health and safety guidelines as well as legal obligations.
  • Supervise inspectors, technicians and other staff and provide guidance and feedback.
  • Oversee all product development procedures to identify deviations from quality standards.
  • Inspect final output and compare properties to requirements.
  • Approve the right products or reject defectives.
  • Keep accurate documentation and perform statistical analysis.
  • Solicit feedback from customers to assess whether their requirements are met.
  • Submit detailed reports to appropriate leadership team personnel.
  • Be on the lookout for opportunities for improvement and develop new efficient procedures.
  • Uphold the Company Quality Policy.


REQUIREMENT SUMMARY

Min:5.0Max:7.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Clinical Pharmacy

Diploma

Business, Engineering

Proficient

1

Litchfield, MI, USA