Jobs at Amneal Pharmaceuticals

Leads national pharmaceutical sales activities for Parkinson’s disease regions, managing Regional Business Managers and specialty sales teams. Responsibilities include sales performance, coaching, recruiting, training, analytics, budgeting, planning, product launches, KOL and MDS relationships, field reviews, and cross-functional alignment with commercial, marketing, analytics, and managed markets teams. Requires extensive pharmaceutical sales leadership experience and 75%–100% overnight travel.

Leads global financial planning, forecasting, reporting, and advanced analytics for a biosimilars portfolio. Partners with Commercial, R&D, Supply Chain, and Business Development teams on pricing, contracting, market selection, profitability, investment, and long-range planning decisions. Develops scenario models, identifies risks and opportunities, improves financial processes and data quality, and provides actionable recommendations to senior leadership.

Leads sterile pharmaceutical manufacturing process transfers from concept through commercial launch, including scale-up, aseptic process simulation, validation, troubleshooting, and continuous improvement. Develops protocols, technical plans, SOPs, batch records, and manufacturing instructions while ensuring FDA and cGMP compliance. Serves as a subject matter expert for formulation, filling, packaging, lyophilization, contamination control, and equipment systems. Manages investigations, change controls, CAPA, risk assessments, vendor collaboration, training, and process capability improvements.

Drive product sales within an assigned territory by presenting approved materials to healthcare practitioners, hospitals, pharmacies, clinics, and retail or wholesale accounts. Manage territory planning, customer calls, samples, sales reporting, compliance documentation, and sales data analysis. Build professional relationships, demonstrate disease-state expertise, maintain accurate Veeva records, attend training and meetings, and provide occasional weekend patient-program coverage. The role requires 50% travel and may include overnight travel.

Coordinates Coupa purchasing for Kentucky facilities, including requisitions, purchase orders, receiving, invoice resolution, vendor setup, compliance, and supply inventory. Liaises with Finance, Procurement, Accounts Payable, vendors, and internal teams; supports month-end activities, accruals, GL coding, and reporting. Tracks departmental projects, timelines, action items, risks, and documentation while supporting Logistics and Distribution operations and process implementation.

Leads corporate development initiatives including M&A, licensing, joint ventures, and strategic alliances. Responsibilities include financial analysis, valuation modeling, due diligence, stakeholder and external partner coordination, transaction execution, acquisition integration, capital planning, SEC filing support, and post-deal performance analysis. The role partners with Finance, Legal, Commercial, R&D, Supply Chain, and executive leadership and requires frequent travel.

Promote pharmaceutical products within an assigned territory by presenting approved product information to healthcare providers and related accounts. Meet sales goals through territory planning, customer calls, data analysis, sample distribution, and relationship building. Maintain accurate records in Veeva, comply with PDMA and company policies, complete administrative reporting, participate in training, and provide occasional patient-program coverage. The role requires 50% travel and may include overnight travel.

Build and deploy production machine learning, forecasting, optimization, and agentic AI systems for pharmaceutical commercial decisions. Develop pricing, contracting, customer profitability, portfolio, market access, and revenue models; create LLM applications for document extraction and intelligence workflows; monitor model performance and data quality; validate business impact with Finance; and present recommendations to commercial leadership.

Designs, programs, qualifies, supports, and improves automation and control systems for sterile pharmaceutical manufacturing. Responsibilities include PLC, HMI/SCADA, DCS, BMS/EMS, instrumentation, networking, commissioning, qualification, troubleshooting, change control, data integrity, documentation, vendor coordination, and cross-functional project execution. The engineer supports cGMP compliance, FAT/SAT, IQ/OQ/PQ, CAPA, lifecycle management, training, and reliable operation of manufacturing and packaging systems.

Build and deploy production AI systems for scientific and regulatory applications, including NLP, document intelligence, generative AI, retrieval-augmented generation, and agentic workflows. Develop validation and evaluation frameworks, production Databricks pipelines, and traceable systems meeting GxP and 21 CFR Part 11 requirements. Support regulatory risk analysis, labeling, literature and patent mining, and product development decisions while communicating technical results and limitations to R&D and Regulatory Affairs leadership.

Leads Amneal’s compliance operations, including global policy and SOP governance, compliance training, U.S. third-party due diligence, and monitoring programs. Advises colleagues on compliance requirements, coordinates cross-functional policy development, manages training records and due diligence reviews, develops monitoring plans, analyzes results, and oversees remediation activities. Requires pharmaceutical industry compliance, legal, or audit experience and knowledge of applicable healthcare compliance laws and guidance.

Supports quality systems and regulatory compliance in a pharmaceutical distribution center. Prepares and reviews batch/distribution documents, manages customer returns and inventory statuses, assists with sampling, shipping studies, environmental and pest control programs, issues controlled forms/logbooks, and helps prepare for audits to ensure cGMP and FDA compliance and product integrity.

Provide technical leadership and hands-on support for sterile manufacturing (BFS, syringes, bag filling, filtration, aseptic processing). Lead validation lifecycle (PPQ, CPV), tech transfer, scale-up, investigations, CAPAs, control strategies, and process improvements. Partner with cross-functional teams on equipment qualification, change control, documentation, audits, and regulatory inspections. Coach junior staff and ensure compliant, robust sterile operations and continuous improvement.

Lead strategic planning, design, and delivery of commercial training for biosimilars and 505(b)(2) products. Create multi-year curricula and blended learning, run onboarding and launch readiness, assess field execution via ride-alongs, manage vendors and budget, partner cross-functionally, oversee LMS certifications, and supervise one events specialist to ensure salesforce proficiency and performance.

Sales Representative responsible for achieving product sales goals across an assigned territory. Duties include presenting products to healthcare providers and accounts, planning customer calls, managing samples under PDMA guidelines, analyzing sales data, maintaining territory records, entering activities in Veeva, completing reports, and ensuring compliance. The role requires life sciences industry experience, frequent customer engagement, and 50% travel, including possible overnight travel and occasional weekend patient-program coverage.

Leads post-approval pharmaceutical projects from initiation through stability, regulatory filing, approval, and commercial implementation. Coordinates R&D, manufacturing, supply chain, procurement, regulatory affairs, operations, vendors, and other cross-functional teams. Supports portfolio selection, alternate-source and cost-saving initiatives, business development, financial modeling, due diligence, forecasting, and market intelligence for generic pharmaceutical products.

Lead and manage end-to-end payroll operations for weekly and bi-weekly payrolls (2,400+ employees), ensure compliance and reconciliations, handle exceptions and off-cycle payments, support audits and SOX controls, produce payroll reports and tax/year-end support, and partner with HR/Finance on system/process improvements (ADP WFN, UKG).

Leads pharmaceutical brand marketing strategy and product launches across HCP and consumer audiences. Responsibilities include positioning, messaging, segmentation, omnichannel and digital campaigns, market access integration, advisory boards, conferences, field readiness, cross-functional launch governance, budgeting, forecasting, vendor management, performance optimization, and team leadership throughout the product lifecycle.

Build and manage partnerships with neurology thought leaders, patient advocacy groups, and academic institutions across headache and Parkinson’s disease portfolios. Support scientific exchange, educational initiatives, product launches, and portfolio promotion. Collaborate with sales, marketing, medical affairs, compliance, and commercial operations teams to develop resources, guide field initiatives, and measure program performance. The role requires pharmaceutical industry experience, therapeutic-area knowledge, and familiarity with regulatory and compliance requirements.

Supervise and schedule QA sampling/inspection for raw materials, in-process and finished products; train and evaluate QA staff; manage SOPs, cGMP compliance, CAPA, deviations, audits, investigations, validations, and customer complaint handling across shifts.