2 часа назад
Lead Development Engineer (Bioprocessing)
87 000 - 100 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Lead Development Engineer (Bioprocessing): Leading mechanical product development for bioprocessing equipment from concept through commercial release with an accent on design refinement, engineering documentation, manufacturability, and product reliability. Focus on developing mechanical assemblies, managing design changes and traceability, conducting prototype testing, and solving technical challenges while mentoring junior engineers.
Location: On-site in Marlborough, Massachusetts, United States, with occasional work in Shrewsbury, Massachusetts
Annual salary: $87,000–$100,000, plus eligibility for bonus or incentive pay.
Company
operates Cytiva, which develops solutions for life sciences, diagnostics, biotechnology, and bioprocessing applications.
What you will do
- Lead the design, development, and refinement of mechanical components, assemblies, and systems for bioprocessing equipment.
- Create and review engineering drawings, specifications, 3D models, and other design outputs using CAD tools.
- Maintain bills of materials in MRP/ERP systems and lead engineering change requests and orders.
- Define design inputs and maintain traceability across requirements, design outputs, risk management, and verification activities.
- Lead project technical activities, facilitate design reviews, resolve engineering challenges, and mentor junior engineers.
Requirements
- Bachelor’s degree in Mechanical Engineering or a related field.
- At least 3 years of product development experience.
- Proficiency in engineering documentation, product development processes, mechanical design principles, GD&T, and tolerance stack-up analysis.
- Hands-on experience with prototype fabrication and testing, including metal and plastic fabrication, assembly, fasteners, welding, 3D printing, troubleshooting, and hardware evaluation.
- Ability to independently execute engineering projects, perform technical analysis, support risk management and root-cause investigations, and collaborate with suppliers and manufacturing partners.
Nice to have
- Master’s degree in a related field.
- Experience with bioprocessing equipment, life sciences, medical devices, industrial equipment, or other regulated products.
- Experience with Creo, PLM/PDM systems, FEA, and applicable product safety and regulatory standards.
Culture & Benefits
- Continuous improvement environment supported by the Business System.
- Medical, dental, and vision insurance for eligible employees.
- Paid time off and 401(k) benefits for eligible employees.
- Opportunity to contribute to products supporting biological research, vaccines, medicines, and cell and gene therapies.
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