US Pharmacopeia
1001 - 5000 employees
Founded 1820
💊 Pharmaceuticals
🧬 Biotechnology
🤝 Non-profit
Pharmaceuticals • Biotechnology • Non-profit
US Pharmacopeia is a non-profit scientific organization that develops and publishes public quality standards, reference materials, and analytical guidance for medicines, dietary supplements, and food ingredients to protect patient and consumer safety worldwide. USP provides over 7,000 reference standards, verification and audit programs, training and technical guidance (including for biologics, gene therapies, and impurities), and data-driven tools to strengthen medicine supply chains and regulatory predictability.
Scientific Affairs Manager
🕒 April 17
🐊 Florida, New Hampshire, +5 more states – Remote
💵 $112.7k - $146.9k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
👔 Manager
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US Pharmacopeia
1001 - 5000 employees
Founded 1820
💊 Pharmaceuticals
🧬 Biotechnology
🤝 Non-profit
Pharmaceuticals • Biotechnology • Non-profit
US Pharmacopeia is a non-profit scientific organization that develops and publishes public quality standards, reference materials, and analytical guidance for medicines, dietary supplements, and food ingredients to protect patient and consumer safety worldwide. USP provides over 7,000 reference standards, verification and audit programs, training and technical guidance (including for biologics, gene therapies, and impurities), and data-driven tools to strengthen medicine supply chains and regulatory predictability.
📋 Description
• Provide scientific guidance on the application and adoption of USP–NF monographs, general chapters, and compendial analytical methods • Advice on the selection, qualification, and lifecycle management of USP Reference Standards • Provide support and technical input to stakeholders on impurity profiling • Build and sustain collaborative relationships with industry, regulators, academia, and scientific associations • Monitor evolving scientific and regulatory trends across pharmaceutical R&D • Collaborate cross functionally with science, marketing, regulatory, and strategic customer development teams
🎯 Requirements
• Master’s degree with 6-8 years, or Ph.D. with 4–6 years of experience in Life Sciences, Chemistry, Biochemistry, Pharmaceutical Chemistry, Biotechnology, or a related discipline • Minimum of 2 years of experience working in pharmaceutical or biopharmaceutical development, quality, regulatory science, or analytical sciences • Knowledge of various analytical testing procedures and methodologies, and regulatory knowledge (FDA, ICH, etc.) for approval of bio-/pharmaceutical products • Demonstrated expertise in pharmaceutical analytical sciences, with strong working knowledge of USP–NF compendial standards, analytical methods, and reference standards • Strong understanding of impurity control strategies • Proficiency in English is required
🏖️ Benefits
• company-paid time off • comprehensive healthcare options • retirement savings
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