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4 дня назад

Engineering Specialist, Facilities and Critical Systems (Pharmaceutical Manufacturing)

152 000 - 209 000$
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
Engineering Specialist, Facilities and Critical Systems (Pharmaceutical Manufacturing): Developing engineering standards and supporting facility, utility, and capital projects for pharmaceutical manufacturing sites with an accent on critical systems, regulatory compliance, and facility reliability. Focus on reviewing designs, solving complex utility performance issues, guiding capital projects, and improving energy efficiency across a global manufacturing network.

Location: Deerfield, Illinois, United States. Domestic and international travel of up to 25% is required. Applicants must be authorized to work for any employer in the U.S.; visa sponsorship is not available.

Salary: $152,000–$209,000 annually, plus potential discretionary bonuses.

Company

hirify.global develops healthcare products and supports manufacturing operations focused on saving and sustaining lives.

What you will do

  • Develop and maintain engineering standards and guidance for facilities, utilities, and capital projects.
  • Provide technical expertise for pharmaceutical facility and critical utility systems.
  • Review facility designs, engineering studies, project plans, and technical solutions for standards and regulatory alignment.
  • Support manufacturing sites with facility upgrades, capital planning, project gate reviews, and projects from concept through startup and turnover.
  • Evaluate system performance and recommend improvements to reliability, energy efficiency, sustainability, and carbon reduction.
  • Partner with manufacturing, maintenance, purchasing, and project teams while mentoring engineering teams across the organization.

Requirements

  • Bachelor's degree in Mechanical Engineering or a related field.
  • 15+ years of experience in pharmaceutical facility, utility, or systems engineering, including 3+ years supporting manufacturing operations.
  • 8+ years in an engineering leadership or senior technical engineering role.
  • Experience applying cGMP requirements in regulated manufacturing and knowledge of FDA, OSHA, 21 CFR, ISO, building, safety, environmental, ISPE, ASME, NFPA, and EPA requirements.
  • Knowledge of HVAC, WFI, compressed air, mechanical, electrical, plumbing, structural, and energy management systems.
  • Experience with facility design, construction management, capital project execution, engineering standards, governance programs, and tools such as AutoCAD or Revit.

Nice to have

  • Experience with Lean Manufacturing, Six Sigma, TPM, or other continuous improvement methodologies.

Culture & Benefits

  • Professional development opportunities and paid volunteer time.
  • Matching charitable contributions, wellbeing programs, and resources for working parents and caregivers.
  • Medical and dental coverage starting on day one for eligible roles.
  • 401(k) retirement plan with employee contributions and company matching, ESPP, flexible spending accounts, and educational assistance.
  • Paid holidays, 20–35 days of paid time off based on tenure, family and medical leave, and paid parental leave.

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