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8 дней назад

Wknd QC Inspector (Manufacturing) - Night Shift

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

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TL;DR
Wknd QC Inspector (Manufacturing) - Night Shift (Quality Control/Manufacturing): Performing in-process and finished-goods inspections, audits, and testing for specialty materials with an accent on product specifications, test equipment, documentation, and nonconformance reporting. Focus on coordinating shop-floor QC activities, maintaining calibrated equipment and records, and supporting validation and continuous improvement in a manufacturing environment.

Location: Onsite manufacturing role; Friday-Sunday, 6:00pm-6:00am. hirify.global is headquartered in Alpharetta, Georgia.

Company

hirify.global manufactures specialty materials and engineered solutions for filtration, healthcare, sustainable packaging, and other industrial applications.

What you will do

  • Perform audits and testing of in-process and finished goods according to product requirements and technical specifications.
  • Coordinate shop-floor QC testing with production schedules and conduct visual inspections of coated, slit, and converted materials.
  • Record test results in the Scapa ERP system and maintain product master files, QC documentation, and Good Documentation Practice records.
  • Issue nonconformance reports and supplier complaints for materials that do not meet specifications.
  • Set up, maintain, and monitor the calibration status of QC test equipment and manage QC laboratory inventory.
  • Support quality engineers and technicians with gauge R&R, validation activities, employee training, and continuous improvement events.

Requirements

  • At least 2 years of experience in a manufacturing Quality Assurance or Quality Control environment.
  • High school diploma required; a bachelor's degree is highly preferred.
  • Knowledge of basic measurements, test equipment, and mathematics.
  • Ability to communicate and collaborate effectively in a team environment.
  • Ability to follow safety, cleanliness, attendance, and documentation requirements.

Nice to have

  • Experience in medical device or industrial manufacturing.
  • Associate degree in chemistry, physical sciences, or a technical field.
  • Experience with gauge R&R, validation activities, or quality documentation.

Culture & Benefits

  • Competitive and affordable benefits with options designed for employees and their families.
  • Work within a global manufacturing organization serving customers across nearly 100 countries.
  • Participate in cross-functional quality and continuous improvement activities.

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