For consideration of any open positions, please send your resume to:
HRDEPT@i-mabbiopharma.com

Description:

I-Mab (Nasdaq: IMAB) is an innovation-driven global biopharma company focused on the discovery, development and commercialization of novel and highly differentiated biologics for immuno-oncology and autoimmune diseases. The Company's mission is to bring transformational medicines to patients around the world through innovation. I-Mab's globally competitive pipeline of more than 15 clinical and pre-clinical stage drug candidates is driven by its internal discovery and global partnerships for in-licensing, based on the Company's Fast-to-Proof-of-Concept and Fast-to-Market development strategies. The Company is progressing from a clinical stage biotech company into a fully integrated global biopharmaceutical company with cutting-edge R&D capabilities, a world-class GMP manufacturing facility and commercial capability. I-Mab has offices in Beijing, Shanghai, Hangzhou and Hong Kong in China, and Maryland and San Diego in the United States. For more information, please visit http://ir.i-mabbiopharma.com and follow I-Mab on LinkedIn, Twitter and WeChat.

This Sr. medical device engineer will be a key contributor in commercial drug delivery device development, lab tests, design control, contract manufacturing (CMO), tech transfer, device related qualifications and continuous improvement in San Diego, California.

Location: San Diego, California

Responsibilities:

• Drug delivery system development in medical devices, such as manual injectors, autoinjector/pen and wearable devices.
• SME from developing commercial devices, product launch to lifecycle support.
• Accountable in developing test methods and generating test protocols independently.
• Other device related activities can be assigned upon device development’s needs.
• Domestic and international travels are required upon business needs

Qualifications:

• Minimum of BS in Science or Engineering, Mechanical Engineering or Electric Engineering is preferred.
• 4+ years of experience for BS and 2+ years of experience for MS or PhD in device tests, device commercialization, filling and packaging processes, or equivalent combination of education and experience. 
• Ability to review engineering drawings and other documents.
• Familiar with the standards and regulations: Quality System Regulation – 21CFR820, ISO 13485 and ISO 11608.
• Excellent (technical) written and verbal communication
• Global team player