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US Pharmacopeia

Director, Digital Reference Standards Products – Partnerships

US Pharmacopeia

. Own the strategy, development, delivery, and adoption of Digital Reference Standards products, including USP-ID .

Posted 9/25/2026full-timeRemote • United StatesLead💰 $171,833 - $243,289 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in product management for Digital Reference Standards, with a strong focus on scientific software development, customer needs translation, and regulatory compliance. Capable of leading cross-functional teams and managing external partnerships to drive product strategy and execution.

Highest-signal resume keywords
Product ManagementScientific Software DevelopmentRegulatory ComplianceCustomer Needs TranslationAnalytical Laboratory Workflows

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Analytical ChemistrySoftware Requirements DefinitionRoadmap DevelopmentUser Acceptance TestingRisk AssessmentProduct Vision and StrategyBudget ManagementLicensing ArrangementsGxP ComplianceNMR or qNMR Experience
Soft Skills
Judgment in Risk IdentificationCommunication with Non-SpecialistsCollaboration Across Stakeholders
Certifications & Qualifications
Bachelor's Degree in Related DisciplineMaster's Degree or PhD (Desired)MBA (Desired)
Industry Keywords
Digital Laboratory ProductsPharmaceutical R&DAnalytical DevelopmentQuality ControlScientific Model LibrariesLaboratory InformaticsRegulated Life Science Product DevelopmentStandard Setting OrganizationRegulatory AgencyPharmaceutical Company

About the role

Key responsibilities & impact
  • Own the strategy, development, delivery, and adoption of Digital Reference Standards products, including USP-ID
  • Define product vision, strategy, roadmap, target use cases, value proposition, success measures, and investment recommendations
  • Convert customer observations, validation findings, scientific limitations, and regulatory expectations into requirements, acceptance criteria, development priorities, and evidence plans
  • Manage software development and integration roadmaps, backlog prioritization, release planning, user acceptance testing, defect resolution, documentation, knowledge transfer, and business continuity planning
  • Serve as the primary product-management counterpart for external developers, integration partners, distributors, and technical collaborators
  • Establish operating cadences, shared deliverables, decision rights, and escalation pathways with partners
  • Partner with Science and Quality on validation readiness, controlled documentation, traceability, risk assessment, remediation planning, and product claims
  • Lead customer discovery, lighthouse collaborations, demonstrations, trials, onboarding, support escalation, and post-trial learning
  • Lead pricing, packaging, channel strategy, forecasts, budgets, contracts, licensing arrangements, and partner economics
  • Support governance through executive updates, KPI and risk reviews, decision documentation, and product and partner knowledge repositories
  • Contribute product perspectives to the Digital Standards strategy and scientific framework
  • Provide functional leadership across scientific, quality, technology, marketing, commercial, and external partner contributors
  • Supervise the Program Manager, Digital Standards

Requirements

What you’ll need
  • Bachelor's degree in analytical chemistry, chemistry, chemical engineering, pharmaceutical sciences, cheminformatics, scientific computing, or a related discipline
  • Ten or more years of relevant professional experience, including substantial responsibility for scientific software, digital laboratory products, analytical technologies, or regulated life science product development or customer acquisition
  • Experience identifying and articulating customer needs and product-market fit in a scientific software context
  • Experience translating customer needs into software requirements, acceptance criteria, and roadmap decisions
  • Experience managing external software development, technology, distribution, or commercialization partners
  • Experience coordinating across scientific, quality, legal, commercial, and executive stakeholders in a matrixed organization
  • Working knowledge of analytical laboratory workflows and performance concepts including accuracy, precision, reproducibility, robustness, traceability, and fitness for purpose
  • Ability to explain technical risks, evidence gaps, and strategic choices to non-specialists
  • Demonstrated judgment in identifying, documenting, and escalating product, supplier, quality, architectural, and commercial risks
  • Remote employees must reside in MD, VA, DC, PA, WV, CA, MI, IL, KS, FL, NC, or MN
  • Desired: Master's degree, PhD, PharmD, or MBA
  • Desired: Hands-on NMR or qNMR experience, or knowledge of quantum mechanical spectral analysis, chemometrics, spectral informatics, or scientific model libraries
  • Desired: At least four years of product management or product owner experience
  • Desired: Experience developing or commercializing software for pharmaceutical R&D, analytical development, process chemistry, manufacturing, or quality control
  • Desired: Experience with software used in GxP or other regulated environments, including electronic records, audit trails, user permissions, validation documentation, change control, or 21 CFR Part 11
  • Desired: Experience operationalizing licensing, distribution, co-development, intellectual property, or strategic partnership agreements
  • Desired: Experience in a standard setting organization, regulatory agency, pharmaceutical company, scientific software company, analytical instrument company, or laboratory informatics business

Benefits

Comp & perks
  • Company paid time off
  • Comprehensive healthcare options
  • Retirement savings
  • Target annual bonus (percentage varies based on level of role)