Quality Coordinator, Medical Devices & Compliance

Orchid MPS Holdings, LLC

Detroit (MI)

Vor Ort

USD 55.000 - 85.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Comprehensive benefits package
Performance bonuses
401(k) with company match
Paid time off

Zusammenfassung

Orchid MPS Holdings, LLC is seeking a Quality Coordinator to support document control, calibration, and inspection activities at the Farmington Hills, MI site. The role emphasizes maintaining the quality system and training records to ensure FDA-compliant practices for orthopedic implants.

You will collaborate with cross-functional teams on quality planning, supplier quality, and corrective actions, contributing to continuous improvement and accurate measurement program management.

Qualifikationen

  • High School diploma or equivalent is required.
  • 3+ years of quality systems experience in a regulated industry preferred.
  • Experience with FDA guidelines and compliance practices.
  • Strong organizational skills and attention to detail.

Aufgaben

  • Lead document control activities and maintain logs.
  • Support training programs and regulatory requirements.
  • Coordinate calibration and metrology, including data collection.
  • Inspect parts using precision measuring equipment.
  • Assist quality team with implementing and using measuring tools.
  • Participate in audits and supplier quality improvements.
  • Read drawings to develop and maintain inspection plans.
  • Track quality metrics and drive continuous improvement.

Kenntnisse

Accuracy and attention to detail
Data analysis tools
ISO 9001 knowledge
Organization
Computer knowledge

Ausbildung

High School Or Equivalent

Jobbeschreibung

Orchid MPS Holdings, LLC is seeking a Quality Coordinator to support document control, calibration, and inspection activities at the Farmington Hills, MI site. The role emphasizes maintaining the quality system and training records to ensure FDA-compliant practices for orthopedic implants.

You will collaborate with cross-functional teams on quality planning, supplier quality, and corrective actions, contributing to continuous improvement and accurate measurement program management.

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