Назад
Company hidden
10 часов назад

Final Release Specialist - 2nd Shift

22 - 31$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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
Final Release Specialist - 2nd Shift (Medical Device Manufacturing): Reviewing and completing manufacturing records for compliant batch final release with an accent on quality documentation, product verification, and regulatory requirements. Focus on identifying nonconformances, tracking deviations and CAPAs to closure, and coordinating record flow across Quality, Operations, Engineering, and other departments.

Location: Devens, MA, United States; onsite, Monday through Friday, 3:00 pm–11:00 pm

Hourly pay: $22.60–$31.00, plus a 10% shift differential where applicable

Company

hirify.global develops and operates industrially scalable laser metal additive manufacturing, precision machining, and digital production infrastructure for aerospace, defense, medical, and other essential industries.

What you will do

  • Set up, organize, review, and complete technical, batch, and final release records.
  • Assign and track work-in-progress records through completion and manage turnaround priorities with Program Managers.
  • Verify batch inspections and physical products before final disposition.
  • Identify, initiate, document, and track nonconformances, deviations, CAPAs, errors, and quality variances to closure.
  • Coordinate with Operations, Customer Service, Distribution, Engineering, Program Management, and other stakeholders to resolve documentation and release issues.
  • Develop and release controlled work instructions and identify improvements to the Final Release process.

Requirements

  • 3+ years of experience in medical device manufacturing with direct responsibility for Final Release or Document Control.
  • Experience reviewing Device History Records and Batch Records for completeness and compliance.
  • Ability to read and interpret engineering drawings, blueprints, and technical specifications.
  • Experience initiating, documenting, and tracking nonconformances, deviations, and CAPAs to closure.
  • Knowledge of ERP and QMS electronic systems.

Culture & Benefits

  • Medical, dental, vision, and life insurance.
  • Generous paid time off.
  • 401(k) plan with company match.
  • Competitive salary and equity package based on skills, qualifications, and experience.
  • Collaborative, inclusive environment focused on quality, accountability, ownership, and continuous learning.

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 →