5 дней назад
Process Engineer - Life Sciences
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Process Engineer - Life Sciences (GMP/GxP Manufacturing): Defining process requirements, equipment needs, operational workflows, and facility design inputs for regulated life sciences manufacturing facilities with an accent on process flows, unit operations, equipment layouts, and capacity planning. Focus on translating pharmaceutical and biotechnology manufacturing processes into compliant facility designs, coordinating multidisciplinary engineering teams, and resolving complex design challenges from early planning through construction support.
Location: Raleigh, NC, United States
Company
Design & Engineering is a full-service architecture, engineering, and design firm working as part of Clayco's integrated design-build organization on complex life sciences and industrial projects.
What you will do
- Lead or support process definition and design for life sciences manufacturing facilities from early planning through construction support.
- Define process flows, unit operations, equipment requirements, capacity needs, and space requirements for regulated manufacturing operations.
- Develop process narratives, block flow diagrams, equipment layouts, and engineering criteria that guide architectural and engineering design.
- Collaborate with clients, process architects, utilities, mechanical, electrical, automation, architectural, and construction teams.
- Contribute to proposals, technical narratives, planning concepts, client workshops, and multidisciplinary design reviews.
- Review process-related deliverables and support compliance with applicable GMP/GxP requirements and industry guidelines.
Requirements
- Bachelor's degree in Chemical Engineering, Biochemical Engineering, Mechanical Engineering, or a related technical field.
- 10+ years of life sciences manufacturing process engineering experience in pharmaceutical, biotechnology, or advanced therapy environments.
- Experience with at least one major modality, including monoclonal antibodies, fill-finish, ATMPs, cell and gene therapies, mRNA, vaccines, APIs, or oral solid dosage.
- Strong understanding of regulated manufacturing processes, unit operations, equipment, facility design inputs, and equipment layouts.
- Familiarity with GMP/GxP environments and regulatory expectations, plus strong client-facing communication and multidisciplinary collaboration skills.
- Experience in design-build or fast-track project delivery is preferred; Professional Engineer licensure is preferred but not required.
Nice to have
- Experience across multiple life sciences modalities, platforms, or production technologies.
- Professional Engineer (PE) licensure.
Culture & Benefits
- Collaborative design-build environment spanning development, design, engineering, and construction.
- Work on creative, complex, award-winning, high-profile projects for clients nationwide.
- Medical, dental, and vision insurance, 401(k), paid time off, and paid company holidays.
- Flexible spending accounts, life insurance, disability coverage, employee assistance, and learning and development programs.
- Discretionary annual bonus based on company and individual performance.
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