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Quality Control Lead (Medical Technology)

Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Quality Control Lead (Medical Technology): Managing site-wide QMS activities and overseeing incoming inspection, in-process checks, final product release, and stock verification with an accent on training compliance, controlled quality documentation, and audit readiness. Focus on coordinating nonconforming material activities, supporting root-cause investigations, and driving quality improvements across Operations, Supply Chain, and Quality Engineering.

Location: Vista Manufacturing Center, Vista, California, United States; onsite

Company

hirify.global develops clinically differentiated medical technologies, products, services, and integrated solutions for orthopedics and active lifestyles.

What you will do

  • Administer the site training program, coordinate assignments, track completion, and support training effectiveness evaluations.
  • Update controlled procedures, work instructions, and quality documentation while identifying QMS gaps and supporting corrective and preventive actions.
  • Prepare records and evidence for internal audits, customer audits, and regulatory inspections, and support follow-up activities.
  • Oversee QC activities covering incoming inspection, in-process inspection, final product release, sampling, and inspection-result verification.
  • Conduct stock checks and inventory verification to maintain accurate product status.
  • Coordinate nonconforming material activities, including segregation, documentation, disposition routing, NCMR closure, and root-cause investigations with Quality Engineering, Supply Chain, and Operations.

Requirements

  • High school diploma or equivalent; an associate degree or relevant certification is preferred.
  • At least 3 years of Quality Assurance or Quality Control experience in manufacturing or another regulated environment.
  • Working knowledge of QMS standards, including ISO 9001, ISO 13485, and AS9100.
  • Ability to read technical drawings, specifications, and inspection data; proficiency with inspection tools, techniques, and basic non-destructive examination methods.
  • Experience using ERP systems such as Oracle for transactions and reporting, plus strong communication, documentation, and organizational skills.
  • Must already have full-time work authorization in the United States and be able to maintain it without employer sponsorship.

Culture & Benefits

  • Medical, dental, and vision insurance.
  • Spending and savings accounts and a 401(k) plan.
  • Vacation, sick leave, and holidays.
  • Income protection plans, discounted insurance rates, and legal services.
  • Collaborative work focused on continuous improvement, scientific excellence, and better patient outcomes.

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