Lead Device Development Engineer, Parenteral Systems
Listed on 2026-11-01
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Quality Assurance - QA/QC
Quality Engineering
Viking Therapeutics, Inc. seeks an Engineer of Device Development to own the integrated device development roadmap across the pipeline, partnering with CMC, Drug Product, Analytical Development, Quality, Regulatory Affairs, Clinical, and Supply Chain to deliver device components of parenteral products.
The role executes design control, risk management, verification testing, and DHF content while guiding external partners and ensuring alignment with FDA guidance and ISO standards for VK2735 and
We would love to welcome a new Lead Device Development Engineer, Parenteral Systems to our organisation in CA, United States.
Step into the Lead Device Development Engineer, Parenteral Systems role at Viking Therapeutics, Inc. in CA, United States and grow with us.
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If your experience matches this role, we encourage you to apply.
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