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Seeking a Quality Compliance/Labeling Specialist for a 6-month contract supporting global medical device labeling, IFU development, and regulatory compliance. The role involves creating, reviewing, and maintaining accurate, compliant product labels and marketing claims across international markets, collaborating with Regulatory, Quality, Engineering, and Marketing teams. Requirements include a bachelor’s degree or equivalent, 2–5 years of experience in medical device labeling, knowledge of global regulations like 21 CFR 801 and EU MDR, and strong communication skills. The position offers up to $67/hr, with benefits such as medical, dental, vision, 401(k), and weekly pay. Based in Cupertino, CA, it provides an opportunity to work with a leading organization dedicated to innovation and compliance in the healthcare industry.