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4 дня назад

Senior Maintenance Supervisor (Pharmaceutical Manufacturing)

84 500 - 162 000$
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

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TL;DR
Senior Maintenance Supervisor (Pharmaceutical Manufacturing): Supervising a 15-person maintenance group and improving productivity, safety, quality, and Maintenance Excellence KPIs in a manufacturing and packaging facility with an accent on preventive maintenance, cGMP compliance, CMMS records, and cross-functional coordination. Focus on scheduling maintenance and calibration, analyzing vendor performance, delivering cost savings, and managing continuous improvement projects.

Location: North Chicago, Illinois, United States

Salary: $84,500–$162,000 per year

Company

hirify.global develops medicines and healthcare solutions across immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Supervise a 15-person maintenance organization, including performance evaluation, hiring, succession planning, training, and talent development.
  • Improve workforce productivity, safety, quality, service levels, and Maintenance Excellence KPIs across the manufacturing and packaging facility.
  • Coordinate maintenance and calibration schedules, prioritize work requests, resolve scheduling conflicts, and communicate issues to stakeholders.
  • Maintain CMMS records, job plans, preventive maintenance schedules, and control reports.
  • Lead maintenance continuous improvement projects, support the site maintenance budget, and deliver cost-saving initiatives.
  • Serve as the primary liaison between maintenance, operations, engineering services, and other functional groups.

Requirements

  • Bachelor of Science degree with at least 2 years of relevant experience, or a technical degree with at least 5 years of experience in mechanical, electromechanical, electrical and instrumentation, MRO, or reliability engineering.
  • At least 2 years of experience with cGMP and good documentation practices.
  • Knowledge of P&ID drawings, loop diagrams, one-line schematics, and related technical documentation.
  • Strong technical knowledge, judgment, analytical ability, interpersonal skills, and experience working with diverse internal and external collaborators.
  • Competence with financial systems and fiscal control.
  • Onsite work in North Chicago, Illinois, United States is required.

Nice to have

  • Technical background in healthcare, medical devices, pharmaceutical, biologics, or similar industries.

Culture & Benefits

  • Paid time off, including vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) benefits for eligible employees.
  • Eligibility for short-term incentive programs.
  • Work in a regulated manufacturing environment focused on safety, quality, and operational excellence.

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