Penumbra

Temporary Clinical Data Manager needed for 20 hrs/week (6-month assignment, possible extension). Lead data management activities for clinical trials, ensure data quality and regulatory compliance. Requires 5+ years experience with EDC systems like Medidata Rave. Remote US position.

Lead supplier development and qualification initiatives to strengthen supply chain resiliency. Requires 6+ years in supplier engineering, technical degree, and expertise in capability assessments and risk reduction. Based in Alameda.

Field-based Therapy Development Specialist role in Phoenix or Las Vegas driving VTE care pathway optimization across hospital accounts. Partner with physicians and nursing leaders to advance clinical programs. Requires hospital program development and stakeholder engagement experience.

Lead quality improvement as a Principal Quality Engineer in Alameda. Requires 7+ years in medical device Quality Engineering, Lean Six Sigma expertise, and FDA QSR/ISO 13485 knowledge. Drive CTQ and cost reduction.

Industrial Engineer II in Cartago to lead Lean initiatives and optimize productivity, capacity, and cost across manufacturing sites. Requires 3+ years in IE or continuous improvement, Lean Six Sigma, and strong data analysis skills.

Join Penumbra in Warsaw as a Customer Service Representative for the UK and Ireland market. Manage the full order-to-cash cycle in SAP, support international customers, and grow within a leading MedTech company. Fluent English required.

Senior SAP Basis Administrator needed in Cartago to ensure stability, security and performance of SAP S/4HANA and HANA cloud environments. Requires 8+ years of SAP Basis experience and advanced English.

Join Penumbra's Production team as a Material Handler I on swing shift in Roseville. Maintain accurate inventory and Kanban levels in a cleanroom environment. Requires GED, 1+ year manufacturing experience, and computer skills.

Lead QC inspection team in Cartago as Quality Supervisor II. Requires engineering degree, 4+ years quality experience, B2 English, and knowledge of FDA QSRs and ISO standards. Strong leadership and problem-solving skills essential.