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20 часов назад

Supervisor, Manufacturing (Medtech)

77 000 - 128 300$
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
Supervisor, Manufacturing (Medtech): Leading day-to-day manufacturing operations for medical device production with an accent on safety, quality, regulatory compliance, and productivity. Focus on supervising production personnel, driving Lean Manufacturing and continuous improvement initiatives, and maintaining FDA- and ISO-compliant processes and documentation.

Location: Marlborough, Massachusetts, United States; onsite manufacturing role.

Annual base salary: $77,000–$128,300, plus bonus eligibility.

Company

hirify.global develops medical technologies focused on women's health.

What you will do

  • Lead daily manufacturing operations to achieve safety, quality, delivery, and productivity objectives.
  • Supervise, coach, develop, and evaluate production employees while managing staffing, scheduling, attendance, and performance.
  • Partner with Engineering, Quality, Regulatory Affairs, EH&S, Materials, and other functions to resolve operational issues.
  • Drive Lean Manufacturing, 6S, and continuous improvement initiatives to improve efficiency, reduce waste, and optimize performance.
  • Support process validations, investigations, testing, manufacturing changes, audits, and inspections.
  • Review production metrics and Device History Records while maintaining accurate manufacturing documentation.

Requirements

  • Associate's degree in a technical discipline or equivalent combination of education and experience.
  • At least 3 years of leadership or supervisory experience in manufacturing and 5 years of manufacturing experience.
  • Strong electrical and/or mechanical background, including familiarity with mechanical assembly, equipment, testing, and repair.
  • Experience in FDA-regulated and ISO-certified environments, with knowledge of GMPs, QSRs, and manufacturing best practices.
  • Knowledge of Lean Manufacturing, continuous improvement, auditing, documentation, problem-solving, and Microsoft Office.
  • Ability to maintain compliance with FDA regulations, ISO requirements, GMP standards, and company policies.

Nice to have

  • Experience in a cleanroom manufacturing environment.
  • Experience with Oracle and Agile systems.

Culture & Benefits

  • Work in an environment focused on safety, quality, teamwork, and continuous improvement.
  • Support a clean, organized, and safe manufacturing workplace.
  • Annual base salary is bonus eligible.
  • Equal opportunity employment is provided, including consideration for women, minorities, veterans, and individuals with disabilities.

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