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
📊 Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
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
Apply NowSimilar Jobs
🕒 April 17
Clinical Applications Manager overseeing MRI clinical activities, managing scanner protocols and driving productivity at Akumin's fixed sites. Supporting technologists and radiologists with QA/QC programs and training.
🕒 April 17
Manager, Trust Services leading global compliance efforts at Workstreet. Overseeing security reviews, legal documents, and team management while working US Eastern Time hours.
🕒 April 17
Manager, Martech improving acquisition systems at Mercer Advisors. Focused on Salesforce, automation, and growth tech operations.
🕒 April 17
Field Organizing Manager leading voter engagement in California through healthcare professionals. Fostering civic engagement and community outreach for Vot-ER initiatives.
🕒 April 17
Senior Renewals Manager driving retention and revenue growth at Appriss Retail. Overseeing subscription renewals and managing complex commercial workloads within a SaaS environment.
