Назад
Company hidden
3 часа назад

Associate Supervisor, Quality (Packaging)

66 000 - 74 000$
Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Associate Supervisor, Quality (Packaging) (FDA/cGMP compliance): Overseeing quality compliance for the handling, packaging, storage, reconciliation, and shipping of finished packaging products with an accent on customer requirements, regulatory compliance, and quality documentation. Focus on creating deviations and validation records, supporting audits, resolving significant quality issues, and managing multiple priority projects.

Location: Edison, New Jersey, United States; primarily working in production and warehouse settings with time in an office

Salary: $66,000–$74,000 annually, plus annual incentive plan and benefits

Company

hirify.global provides corrugated and plastic packaging products and supply chain solutions through Menasha Packaging and ORBIS Corporation.

What you will do

  • Oversee compliance for material movement, storage, reconciliation, segregation, quarantine, destruction, and issuance to production.
  • Ensure handling, packaging, and shipping of finished products meet customer requirements and applicable FDA and cGMP regulations.
  • Create rework protocols, deviations, change controls, nonconformances, validations, and validation tracking documentation.
  • Initiate, review, and approve customer requirements, quality tools and techniques, and Quality Department job descriptions.
  • Support quality batch records, quality control auditing, material release, and Quality Manager responsibilities when needed.
  • Prepare for and support customer and internal audits, improve quality procedures, and resolve significant quality issues with Production and Quality Management.

Requirements

  • Associate’s degree required; Bachelor’s degree preferred.
  • At least two years of combined training, education, or relevant experience.
  • Strong knowledge of FDA regulations, cGMP regulations, and workplace safety.
  • Proficiency with Microsoft Word and Excel, plus communication, management, negotiation, and technical writing skills.
  • Ability to solve problems independently, manage multiple high-priority projects, delegate, and direct others.
  • Ability to travel when necessary and perform prolonged walking, sitting, and standing, including occasional lifting up to 25 pounds.

Nice to have

  • Bilingual Spanish skills.
  • ASQ or another quality certification.

Culture & Benefits

  • Full-time salaried exempt employment.
  • Medical, dental, and vision insurance.
  • Life, AD&D, short- and long-term disability, and employee assistance program coverage.
  • 401(k) retirement savings plan, paid time off, and paid holidays.
  • Annual incentive plan and opportunities for professional growth.

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 →