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11 дней назад

Supervisor, Final Release - Day Shift (Manufacturing Quality)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
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
Supervisor, Final Release - Day Shift (Manufacturing Quality): Leading final release operations for regulated manufacturing products with an accent on documentation accuracy, quality compliance, and production coordination. Focus on supervising records review, inspections, nonconformances, CAPAs, and cross-functional resolution of release issues.

Location: Devens, Massachusetts; five days on-site, Monday through Friday, 7:00 a.m. to 3:00 p.m.

Company

hirify.global develops and operates vertically integrated laser metal additive manufacturing and precision machining capabilities for aerospace, defense, medical, and other essential industries.

What you will do

  • Supervise the Final Release team, assign work, set daily priorities, monitor performance, and coordinate staffing.
  • Oversee manufacturing and technical records through review, inspection, completion, and final disposition.
  • Ensure accurate review of data entry, manufacturing documentation, Device History Records, batch records, and final release documentation.
  • Coordinate correction of incomplete or inaccurate records and escalate quality variances, deviations, nonconformances, and operational issues.
  • Represent Quality and Final Release in production planning meetings and communicate release status, risks, and documentation gaps.
  • Improve workflows, work instructions, training, operational metrics, and Final Release turnaround time.

Requirements

  • At least 5 years of experience in manufacturing, quality assurance, final release, or a related regulated manufacturing environment.
  • Experience leading, coordinating, training, or directing employees in a manufacturing or Quality environment.
  • Experience reviewing Device History Records, batch records, manufacturing records, or similar controlled documentation.
  • Experience identifying, documenting, and tracking nonconformances, deviations, or CAPAs.
  • Ability to interpret engineering drawings, blueprints, technical specifications, work instructions, and controlled documentation.
  • Working knowledge of Quality Management Systems and ERP systems, with strong attention to detail and cross-functional communication skills.

Nice to have

  • Experience in medical device or aerospace manufacturing.

Culture & Benefits

  • Inclusive environment focused on quality, curiosity, accountability, ownership, and continuous learning.
  • 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.

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