Production Supervisor – Weekday Day Shift (1st Shift) (Medical Devices)
Контакты
75 000 - 100 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
team leadershiperpmanufacturinggmpquality managementfdaiso 13485root cause analysisproduction operationsmedical devices
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
Пожаловаться
Зарплата и рынок
Мало
$75к-100к/год
$87к$98кмедиана$100к
По похожим ролям (50) ~ $98к/год
На СНГ рынке: $1.4к/мес ($1.1к - $1.4к)
69
Хорошая вакансия
развернуть
Понятные обязанности, льготы и работа в медицинских технологиях выглядят привлекательно, но зарплатный диапазон ниже рыночной медианы, а возможные переработки добавляют неопределенности графику.
Кликните для подробной информации
Ниже рынкаВозможны переработкиПонятные задачиМедтех с миссией
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Подключить Plus
Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Production Supervisor – Weekday Day Shift (1st Shift) (Medical Devices) (Manufacturing Operations): Leading daily manufacturing operations for the iLet Bionic Pancreas with an accent on production targets, quality systems, safety, and delivery commitments. Focus on supervising and developing production teams, driving continuous improvement, resolving cross-functional production issues, and maintaining FDA, ISO 13485, and GMP compliance.
Location: Irvine, CA, United States; onsite production role. Schedule: 1st shift, Monday–Thursday, 5:00 AM–3:30 PM. Occasional overtime, schedule adjustments, additional weekday coverage, and up to 5% travel may be required.
Salary: $75,000–$100,000 per year
Company
hirify.global is a medical technology company developing the iLet Bionic Pancreas for type 1 diabetes management.
What you will do
Supervise daily manufacturing operations and ensure safety, quality, delivery, and productivity targets are achieved.
Lead, coach, train, and develop production employees through feedback and accountability.
Monitor schedules, staffing, workflow, production metrics, and departmental KPIs.
Drive continuous improvement and implement corrective actions to improve productivity, quality, and operational efficiency.
Collaborate with Quality, Engineering, Supply Chain, Maintenance, and other teams to resolve production issues and support new product introductions.
Maintain production records and support internal, customer, and regulatory audits, investigations, and CAPAs.
Requirements
Knowledge of manufacturing processes, production operations, quality systems, and regulatory requirements in a regulated manufacturing environment.
High School Diploma required; an Associate's or Bachelor's degree in Manufacturing, Engineering, Business, or a related field is preferred, or equivalent experience.
3–5 years of manufacturing experience, preferably in medical devices or another regulated industry.
Strong leadership, coaching, conflict-resolution, problem-solving, root cause analysis, organizational, and communication skills.
Proficiency with Microsoft Office and ERP systems, including the ability to interpret production metrics.
Ability to work in lab, clean room, and warehouse environments and remain independently mobile during the workday.
Nice to have
1–3 years of supervisory or team leadership experience.
Experience with FDA, ISO 13485, GMP, or similar quality systems.
Associate's or Bachelor's degree in Manufacturing, Engineering, Business, or a related field.
Culture & Benefits
Mission-driven, collaborative environment with opportunities for employee development and meaningful impact.
Comprehensive medical and dental coverage.
FSA and HSA plan options, including an annual company HSA contribution.
401(k) program with employer match.
Vacation accrual and paid holidays.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →