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Lead design control and risk management for new and sustaining medical device projects. Maintain risk files per ISO 14971, support verification/validation, usability studies, process qualifications, audits, and QMS procedure updates. Provide technical support for regulatory audits and train staff on quality and QMS principles.

As a Bioprocess Biopharma Account Manager, you will lead customer success, grow sales, develop solutions, and maintain account relationships.

Execute daily production plans and ensure quality compliance, focusing on protein purifications and adherence to established protocols.

The Software Systems Engineer will integrate software systems, manage requirements and cybersecurity, drive automation, and support DevOps practices while collaborating with the software team.

The Senior Clinical Study Manager will oversee clinical trial execution, ensure regulatory compliance, develop study protocols, and drive operational excellence.

The Senior Operations Manager oversees manufacturing performance, ensuring safety, quality, delivery, and cost efficiency, while leading operations leaders and driving continuous improvement initiatives.

This role oversees master data governance, leading a global team and ensuring accurate data management across commercial operations. Responsibilities include strategy development, integration, and continuous improvement of master data quality.

The Senior Project Manager leads complex, global Value & Access initiatives, ensuring execution and governance across cross-functional teams in the diagnostics industry.

The Sr. Technical Product Manager will lead complex initiatives by translating product strategy into software capabilities, manage the product backlog, and ensure alignment with engineering release metrics in a regulated environment.

The Accountant will manage general ledger activities, oversee invoicing, prepare month-end journal entries, and assist with audits and tax documentation.