"fda regulations" Jobs
99 open tech roles matching “fda regulations”, taken straight from company career pages — not reposted from other job boards. Most in demand right now: AI/ML, Python, ISO 13485. Every listing is re-checked daily and closed roles are removed.
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Lead global regulatory affairs for advertising and promotion at a biopharmaceutical company focused on rare diseases.
Lead global regulatory strategy for rare disease clinical development at Mirum Pharmaceuticals.
Join Mirum Pharmaceuticals as an Associate Director in Regulatory Affairs to guide compliant advertising and promotional strategies for rare disease treatments.
Lead global CMC regulatory strategy and execution at Iambic Therapeutics, ensuring compliance and alignment with program objectives.
Join Mirum Pharmaceuticals as a Senior Manager in Regulatory Affairs Labeling to lead global labeling strategy for rare disease treatments.
Lead the establishment of the regulatory affairs function in the US for a company focused on preventative healthcare.
Own the postmarket quality infrastructure for a cfDNA-based colorectal cancer detection test at Freenome.
Lead regulatory strategy for a cutting-edge AI healthcare platform ensuring compliance and safety in patient engagement.
Lead the Quality & Regulatory function at LightForce, driving scalable systems and regulatory strategy in a growing medtech company.
Lead GMP Quality Assurance operations at Mirum Pharmaceuticals, ensuring compliance and product quality for rare disease treatments.
Join Iambic Therapeutics as an Associate Director of Drug Safety, overseeing pharmacovigilance activities in a remote role.
Lead the clinical regulatory affairs at Neko Health, focusing on clinical evaluation and submissions for medical devices.
Lead the regulatory affairs function at insitro, shaping strategies for innovative therapeutics in a pioneering AI-driven biotech environment.
Lead global regulatory strategy and compliance for AI-driven healthcare products at Hippocratic AI.
Join Neko Health as a Regulatory Affairs Engineer to ensure compliance in manufacturing and distribution of medical devices.
Lead quality assurance for medical device hardware and firmware, ensuring compliance and safety in a fast-paced startup environment.
Lead global regulatory strategies for Olema Oncology's products, focusing on innovative therapies for breast cancer.
Lead drug product development and manufacturing for rare diseases at Mirum Pharmaceuticals.
Lead the development and execution of regulatory strategies for Olema Oncology's products as the Director of Global Regulatory Affairs Strategy Lead.
Join Orca Bio as a Statistician to provide statistical leadership in developing next-generation cell therapies.