engineeringmanufacturingprocess engineeringpharmaceutical manufacturingsap pmcapacgmpequipment validationsop writingmaintenance management systems
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
$87к-137к/год
$85к$93кмедиана$100к
По похожим ролям (50) ~ $93к/год
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В Company hidden хорошо описана инженерная роль с ценным опытом в фармпроизводстве, но обязательная работа на месте во вторую смену и ограничения по месту проживания сужают круг тех, кому подойдут условия.
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Вторая сменаЧёткие задачиОпыт в фарме
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Specialist Engineering (Onsite) (Pharmaceutical Manufacturing): Providing onsite engineering support for formulation, filling, facility utilities, and non-sterile manufacturing equipment at a pharmaceutical FLEx center with an accent on GMP compliance, reliability maintenance, and clinical batch availability. Focus on troubleshooting, equipment validation, deviation and CAPA investigations, change management, and commissioning new equipment during second-shift operations.
Location: Rahway, New Jersey, United States; onsite, Monday through Friday on the second shift. The role supports 10% travel and is open to US and Puerto Rico residents only.
Salary: $87,300–$137,400 annually, plus potential annual bonus and long-term incentive.
Company
hirify.global is a pharmaceutical company developing and manufacturing medicines, including clinical, stability, developmental, and commercial Oral Solid Dosage products.
What you will do
Provide onsite engineering and compliance support for facility utilities, manufacturing equipment, and non-sterile pharmaceutical operations.
Maintain equipment availability for clinical and development batches using reliability maintenance practices.
Troubleshoot equipment and partner with GES, Facilities Management, OEMs, vendors, and clinical operations.
Support equipment validation from commissioning through decommissioning, including changes and periodic reviews.
Investigate deviations, issue Quality Notifications, identify root causes and CAPAs, and maintain GMP documentation.
Coordinate equipment installation and commissioning, manage purchase orders and capital requests, and support regulatory interactions as a subject-matter expert.
Requirements
Bachelor’s degree in engineering and at least 2 years of related experience supporting pharmaceutical manufacturing.
Strong familiarity with Quality, cGMP, Safety, and Environmental policies and procedures.
Familiarity with Computerized Maintenance and Management Systems (CMMS).
Ability to adapt across Quality and Facility responsibilities to support business needs.
Effective organizational, communication, and technical writing skills.
Strong computer skills.
Ability to work with minimal supervision during second-shift operations and serve as a technical and compliance resource.
Nice to have
Familiarity with Oral Solid Dosage drug product manufacturing equipment and processes.
Mechanical, electrical, or automation troubleshooting experience.
Maintenance and engineering techniques, maintenance management, and capital project management experience.
Independent problem-solving skills and the ability to lead or facilitate tasks.
Experience with SAP Plant Maintenance, including gatekeeping and work-order prioritization.
Experience with eVal/Kneat, ProCal, planning and scheduling, and business or financial practices.
Culture & Benefits
Regular full-time employment with onsite work at the Rahway FLEx center.
Medical, dental, vision, and other insurance benefits for employees and families.
Retirement benefits including a 401(k), paid holidays, vacation, and compassionate and sick days.
Inclusive workplace focused on collaboration, diverse perspectives, and respectful challenge.
Visa sponsorship is not available; domestic relocation is indicated.
Hiring process
Applications are accepted through the hirify.global careers portal; current employees and contingent workers use the designated internal application links.
US and Puerto Rico residents may request accommodation during the hiring process.
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