Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Роль четко описана и дает возможность отвечать за новый фармацевтический объект на уровне руководства, но работа на месте и командировки на 20% требуют серьезной готовности.
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Командировки и офисРуководящая рольНовый объектПонятные задачи
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Director of Facility Management (Pharmaceutical Manufacturing): Leading facility and utility maintenance, engineering, and asset lifecycle management for a new pharmaceutical drug-substance manufacturing facility with an accent on construction support, regulatory compliance, and operational efficiency. Focus on developing maintenance and calibration programs, managing engineering projects and resources, and improving HVAC, process piping, plant utilities, safety, and production reliability.
Location: Middletown, DE, US; on-site. The role requires 20% domestic and international travel.
Company
hirify.global operates a new approximately 460,000-square-foot facility for manufacturing small-molecule pharmaceutical active ingredients, oligonucleotides, and peptides.
What you will do
Lead facility and utility system operations, maintenance, engineering activities, and asset lifecycle management for drug substance operations.
Provide engineering leadership and allocate resources for construction of the new facility and future engineering projects.
Develop and implement maintenance and calibration programs that meet regulatory requirements and maximize production.
Manage departmental and capital costs, schedules, resources, internal teams, external resources, and project plans.
Develop and execute facility and process improvement plans using new technologies and innovative solutions to improve efficiency, safety, risk management, and costs.
Lead staff performance, development, coaching, corrective action, and coordination with site leaders, designers, and client representatives.
Requirements
Minimum 15 years of relevant experience or equivalent in pharmaceutical maintenance and/or engineering, preferably supporting drug substance operations.
Bachelor’s degree in Engineering or equivalent experience.
Master’s degree and Professional Engineer license preferred.
Strong hands-on leadership style and proficient oral and written communication skills.
Demonstrated ability to read, write, and speak English.
Proficiency in Microsoft Office, including Excel, Word, and Outlook.
Ability to read and approve engineering documentation, calculations, and drawings for HVAC, ductwork, process piping, and plant utilities.
Understanding and implementation of Good Laboratory Practices and Good Manufacturing Practices, applicable regulations, international standards, company policies, and standard operating procedures.
Ability to work in office, indoor, outdoor, variable-temperature, and variable-noise environments; wear appropriate PPE; stand, sit, walk, crouch, bend, twist, reach, climb ladders, stairs, or scaffolding; lift and push/pull 10 pounds routinely, often, or occasionally; distinguish colors; and perform repetitive motions.
Culture & Benefits
Membership in the Site Leadership Team.
Metric-driven leadership aligned with integrity and dedication, collaboration, doing the right thing, and doing it right.
Work supporting construction and operation of a new pharmaceutical manufacturing facility.
Compliance-focused environment covering labor, safety, quality, regulatory, and company requirements.
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