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Production Supervisor (2nd Shift | 3pm - 11pm PST)

70 000 - 88 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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
Production Supervisor (2nd Shift | 3pm - 11pm PST): Supervising medical device manufacturing operations and production teams with an accent on FDA, ISO 13485, GMP, safety, and quality compliance. Focus on executing production schedules, supporting CAPA and nonconformance investigations, and driving Lean, 5S, and continuous improvement initiatives.

Location: On-site in Orange County, California, United States; 2nd shift from 3pm to 11pm PST, with possible weekend coverage and overtime.

Salary: $70,000–$88,000 annually.

Company

hirify.global is a digital healthcare company developing wearable biosensors, cloud-based data analytics, and proprietary algorithms for cardiac monitoring and clinical insights.

What you will do

  • Supervise daily manufacturing operations and ensure production schedules, safety requirements, and quality specifications are met.
  • Lead, motivate, train, and develop manufacturing associates while monitoring performance, attendance, and adherence to procedures.
  • Execute production plans, adjust staffing and resources, and coordinate with planning and supply chain to maintain material availability and optimized inventory.
  • Maintain production records, deviations, maintenance documentation, and Plan vs. Actual performance tracking.
  • Support nonconformance investigations, CAPAs, quality audits, Good Documentation Practices, and data integrity requirements.
  • Conduct safety inspections and participate in Lean events, 5S programs, standardization, and other continuous improvement initiatives.

Requirements

  • Associate degree or equivalent experience required; a bachelor's degree in engineering, manufacturing, or a related field is preferred.
  • 3–5 years of manufacturing operations experience, including 1–2 years in a supervisory or lead role.
  • Experience leading small to medium-sized production teams, preferably in medical device manufacturing or another regulated industry.
  • Working knowledge of ISO 13485, FDA 21 CFR Part 820, GMP, quality systems, and medical device manufacturing.
  • Familiarity with ERP or MRP systems such as QAD, SAP, or Oracle.
  • Regular on-site presence on the manufacturing floor is required.

Culture & Benefits

  • Patient-first mission focused on improving cardiac health outcomes.
  • Collaborative, inclusive, and accountable work environment.
  • Emphasis on continuous learning, knowledge sharing, employee development, and recognition.
  • Commitment to workplace safety, quality, operational excellence, and continuous improvement.
  • Equal opportunity workplace with reasonable accommodations available during the hiring process.

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