Jobs at Harrow

Owns commercial analytics reporting for pharmaceutical commercial operations, including KPI dashboards, territory performance tracking, brand trend analysis, data quality, ad hoc analysis, and incentive compensation support. Builds Power BI dashboards and data models using warehouse, pharmacy, and claims data. Partners with Commercial, Finance, and Market Access stakeholders, develops KPI definitions, supports executive decisions, and mentors junior analytics staff.

Perform QC microbiological testing and data review, manage stability studies and sample inventory, support environmental monitoring, investigations (OOS/OOT), CAPAs, and regulatory compliance under GMP/ICH/FDA standards.

Senior Systems Analyst responsible for analyzing and improving systems, designing AI-driven and automated solutions, implementing software, databases and integrations, overseeing testing and documentation, managing cross-functional projects, and providing advanced user training and technical guidance across the organization.

Manage marketing platforms and the promotional review cycle (PRC) across branded and compounded portfolios. Coordinate, review, and QC promotional materials in Veeva, lead review meetings, ensure regulatory submissions (2253), maintain audit-ready documentation and trademark logs, improve processes/SOPs, train stakeholders, and manage NDCs/labels for compounded products.

Provides administrative support to the Quality Assurance team by handling inquiries, initiating and documenting Product Quality Complaints, maintaining complaint trackers, updating SharePoint and QA records, and supporting document control, filing, archiving, and general QA activities. The role requires accurate procedure-following, confidentiality, communication skills, Microsoft Office proficiency, and willingness to learn pharmacovigilance and compliance principles. This is a remote position with occasional travel up to 10%.

Lead and perform microbiological testing, method qualification/validation, environmental monitoring, and investigations for sterile pharmaceutical manufacturing. Serve as microbiology SME, support regulatory inspections, author and review QC documentation, mentor staff, and drive continuous improvement while ensuring cGMP and USP compliance.

The Quality Assurance Complaints Specialist ensures compliance with manufacturing standards, handles customer complaints, initiates investigations and corrective actions, and maintains documentation.

Manage business for ophthalmology/retina accounts across an assigned territory, secure MBOs, manage GPO contracts, run quarterly business reviews, drive retention and portfolio performance, build executive relationships, collaborate with commercial teams, and travel up to 50%.

Lead pricing and contract lifecycle for ImprimisRx compounded products, including contract loading, validation, renewals, pricing analysis, dashboards, dispute resolution, system configuration, compliance with compounding regulations, audit support, and cross-functional collaboration with Sales, Finance, and Legal.

Lead day-to-day Quality Assurance and Quality Control operations for a 503B compounding facility to ensure cGMP compliance, inspection readiness, batch release, investigations, CAPA, data integrity, and quality metrics. Manage QA/QC teams, partner with manufacturing and supply chain, lead regulatory inspections, and drive continuous improvement.