Jobs at Penumbra

Manages sales growth and customer satisfaction for neurovascular medical devices within an assigned territory. Develops relationships with hospitals, physicians, laboratory staff, purchasing teams, and prospective customers; secures orders; supports product use; monitors inventory and market trends; attends trade shows; maintains sales records; and follows quality, compliance, and regulatory requirements. The role requires up to 50% business travel, occasional on-call availability, and work in office, laboratory, and cleanroom environments.

Acts as a strategic HR advisor to business leaders, providing guidance on employee relations, performance management, compliance, compensation, workforce planning, talent management, and organizational development. Partners with Legal and HR teams, analyzes workforce metrics, leads complex HR initiatives, facilitates training, supports benefits and leave processes, and promotes an inclusive culture. The role requires strong HR expertise, HRIS experience, project leadership, and knowledge of employment regulations.

Develops and executes marketing strategies for medical device products, supporting commercialization, product launches, market research, customer and field support, competitive analysis, product positioning, training, sales tools, and global marketing collaboration. The role works closely with physician customers, sales teams, and cross-functional launch groups while ensuring compliance with quality and regulatory requirements.

Supports marketing programs for neuro fellows and medical societies across the U.S. and Canada. Coordinates events, communications, materials, contracts, timelines, customer engagement, speaker and KOL relationships, field support, competitive intelligence, and cross-functional initiatives. Ensures marketing activities comply with company quality systems, privacy, security, and applicable laws. The role is Alameda-based, requires 50% or more business travel, and includes work in cath labs or operating rooms.

Develop and implement quality system elements for catheter products, supporting product development, testing, inspections, sampling, failure analysis, audits, SOPs, and regulatory compliance. The role partners with engineering teams, customers, and suppliers to resolve quality issues, leads quality initiatives, and provides guidance to junior engineers and interns. Work occurs across office, laboratory, and cleanroom environments with occasional travel.

Supports Quality Management System activities for medical devices, analyzes quality data, investigates nonconformances, identifies root causes, and drives corrective and preventive actions. Partners with cross-functional teams on continuous improvement, product and process validations, regulatory compliance, and quality control to ensure safe, effective products.

Leads and develops the training function supporting Production and Quality. Supervises Training Specialists, builds and administers training systems and programs, improves training initiatives, ensures employee competency and operational compliance, and tracks training metrics and KPIs in a regulated life sciences manufacturing environment.

Drive commercial growth across a UK Midlands and South-West neurovascular territory by acquiring new accounts and expanding existing ones. Responsibilities include territory strategy, forecasting, account segmentation, clinical relationship development, KOL engagement, product demonstrations, clinical education, market analysis, pricing and reimbursement positioning, and cross-functional go-to-market collaboration. The role is field-based and requires independent territory ownership, strong clinical engagement, and effective communication with healthcare professionals.

Develops, implements, delivers, and continuously improves technical training programs supporting production, quality, and operational excellence. Serves as a subject matter expert in training compliance, Lean learning principles, technical certification, and workforce development. Maintains training materials and certification processes while partnering with manufacturing, quality, and continuous improvement functions in medical device, pharmaceutical, or biotech environments.

Implement, support, and enhance Camstar MES solutions, including eDHR rollout, business process modeling, integrations, requirements gathering, data mapping, documentation, solution design, and system improvements. Serve as liaison between IT and business process owners, train users, support MES transactions and screens, manage user stories and success metrics, and promote compliance with quality, security, privacy, and regulatory standards in a medical device manufacturing environment.

Coordinates IT onboarding, employee training, headcount tracking, budgeting, forecasting, vendor relationships, contracts, SLAs, invoicing, reporting, and IT meetings. Partners with HR, Finance, Legal, IT leaders, and suppliers to manage spend, performance, compliance, and process improvements. Supports strategic alignment and initiatives that improve the IT user experience while adhering to quality, security, privacy, and regulatory requirements.

Leads supplier development, qualification, capability assessment, process improvement, and supply risk reduction initiatives. Partners with Procurement, Engineering, Manufacturing, Operations, Quality, and suppliers to improve quality, scalability, process robustness, and supply continuity. Conducts manufacturing evaluations, root cause investigations, corrective actions, readiness assessments, and technical due diligence. Provides technical leadership for supplier programs, mentors team members, and influences cross-functional decisions involving supplier performance, diversification, transfers, and second-source qualifications.

Leads quality engineering for medical device product development and qualification. Responsibilities include design controls, inspection and testing methods, measurement validation, statistical analysis, corrective and preventive actions, quality documentation, SOP development, and support for FDA inspections and notified body audits. The role ensures compliance with QMS requirements, ISO standards, and global quality regulations while coordinating quality activities across development projects.

Supports development and qualification of medical devices by implementing quality systems, designing testing and inspection methods, applying statistical sampling, performing failure and defect investigations, and analyzing design controls. The role ensures compliance with QMS requirements, QSR, ISO standards, and applicable regulations while collaborating with product development teams, internal departments, customers, and suppliers.

Administer and optimize digital asset management and marketing systems, including content governance, intake processes, asset collections, search frameworks, workflows, audits, and compliance. Partner with Marketing, Creative, and IT stakeholders to implement technology enhancements, improve operational efficiency, analyze metrics, and recommend solutions. Develop training and adoption strategies while serving as a subject matter expert in digital asset management, marketing technology, and creative workflows.

Provides enterprise endpoint systems engineering, development, deployment, lifecycle management, automation, and advanced Tier 2/3 support across Windows and Apple environments. Manages MDM, Active Directory, Entra ID, access policies, software deployment, system standardization, infrastructure lab initiatives, vendors, documentation, and operational improvements. Supports acquisitions, compliance, and quality systems while mentoring IT support staff and maintaining employee relationships.

Administers and maintains enterprise collaboration platforms, primarily Microsoft 365, Teams, Zoom, and related applications. Responsibilities include configuration, access management, monitoring, incident escalation, troubleshooting, maintenance, change validation, workflow and automation support, documentation, licensing, compliance controls, vendor coordination, and operational improvements. Provides technical guidance and on-call support while partnering with engineering, security, compliance, quality, business, and support teams.

Support Penumbra's growth in Colombia by executing field medical visits, organizing hands-on sessions and product trainings with distributors and healthcare professionals, driving product launches and adoption, gathering market intelligence, and managing/training distributor staff to align with commercial and clinical strategies.

Administers, implements, optimizes, and maintains enterprise infrastructure across on-premises and cloud environments. Manages Azure, Microsoft 365, Windows and Linux servers, identity services, storage, virtualization, backup and recovery platforms, and related enterprise systems. Leads troubleshooting, root-cause analysis, automation, security governance, capacity planning, patching, and infrastructure improvements. Supports ERP and integration platforms, collaborates with vendors and internal teams, documents complex system designs, and provides rotating after-hours support.

Administers and optimizes enterprise Microsoft SQL Server environments across on-premises and cloud platforms. Responsibilities include performance tuning, security, backups, recovery, high availability, disaster recovery, monitoring, automation, patching, capacity planning, troubleshooting, compliance, documentation, and stakeholder collaboration. The role provides database subject-matter expertise, supports business-critical applications and integrations, participates in on-call coverage, and improves database reliability, scalability, and operational controls.