Top Pharmaceutical Jobs in Madison, WI

Support product development and act as a liaison between product management, development teams, and stakeholders by conducting analysis and documenting business requirements.

The Director of Product Marketing leads product positioning and go-to-market strategies for the Elluminate Clinical Data Platform, collaborating with commercial and product teams to drive revenue growth and enhance market differentiation.

The Sr. Incentives & Strategy Analyst will optimize and evaluate incentive programs, derive insights from data, and collaborate with cross-functional teams to support revenue strategies.

The CARD Health & Science Professional is responsible for increasing sales and developing customer relationships through product promotion and strategic business management.

The Chief Operating Officer will lead operational execution and manage delivery teams, drive company-wide operating rhythms, and partner closely with the CEO and leadership team to scale the organization and enhance operational effectiveness.

Lead global supply chain process excellence by standardizing planning, procurement, inventory, logistics, and technology. Drive Lean/Six Sigma improvements, harmonize KPIs, optimize ERP/MES and advanced planning (MPS/MRP/finite scheduling), host global forums, deploy digital tools, and ensure GMP-compliant, data-driven operations across multi-site pharmaceutical/CDMO environments.

Execute and document cGMP QC testing, review and enter data into LIMS, author SOPs/reports, lead investigations in Trackwise, support process improvements, train staff, and maintain lab and equipment per GMP.

Manage and improve quality systems (investigations, CAPA, change control, OOS), lead cross-functional improvement initiatives, develop and deliver training, maintain controlled documents, and support regulatory compliance in a GMP biologics CDMO.

Lead day-to-day QC laboratory operations, manage and develop QC staff, ensure timely high-quality analytical testing and regulatory compliance, drive investigations and corrective actions, support lab expansion/qualification, implement KPIs and continuous improvements to scale QC for clinical and commercial manufacturing.

Author, edit, and standardize GMP manufacturing QMS documentation including deviations, investigations, CAPAs, and change controls. Ensure records are inspection-ready, data-integrity compliant, and traceable. Coordinate with SMEs and cross-functional teams to translate technical input into clear, evidence-linked narratives and support audits/inspections.

Field-based territory sales role building strategic account plans, solving access and reimbursement challenges, coordinating cross-functionally, and engaging HCPs via omni-channel tactics to drive product demand and improve patient outcomes.

Lead payer and pricing strategy for major national and regional accounts, develop contract and value-based pricing strategies, negotiate and implement customer contracts, manage a team of directors, build senior payer relationships, and drive cross-functional pricing and market access initiatives across a therapeutic area.

Lead US market access strategy for launch and inline brands, develop 3–5 year access plans, coordinate cross-functional execution (pricing, contracting, marketing, legal), manage budgets, vendor RFPs, and ensure payer coverage, affordability, and durable product value.

Support press or laminator setup and production by preparing inks, coatings, and materials; clean and maintain equipment; load/unload cylinders and raw materials; monitor product quality; operate forklifts and parts washers as needed; follow safety procedures and assist operators and supervisors to keep operations running smoothly.

As a QA Associate I, you will support GMP production by ensuring product quality and compliance, conducting inspections, and assisting in investigations.