CAREERS

The Controller will be responsible for managing Theradaptive’s accounting functions, ensuring adherence to all regulatory standards and leading financial reporting and statements, compliance, and auditing. The Controller will provide strategic financial insights to support our growth. This is a part-time, hourly position.

The Accounting Manager will be responsible for overseeing and managing the general accounting function. The Accounting Manager will be responsible for the month-end close process including journal entries, account reconciliations and other accounting related activities. The ideal candidate would bring the capability and desire to support the evolution of our Accounting function in alignment with the growth of our organization.

The Clinical Trial Manager (CTM) is responsible for the strategic planning, execution, and oversight of our spinal fusion clinical trials from initiation to completion. This role ensures that clinical studies are conducted in compliance with regulatory requirements, Good Clinical Practice (GCP) guidelines, and company policies while meeting timelines, budget, and quality objectives.

We are seeking a talented Senior Quality Engineer who is fluent in Japanese and English to ensure that the highest standards of quality and compliance are met for our organization. This position will play a pivotal role in establishing and maintaining robust quality systems and processes to support our first-ever clinical trials through to our manufacturing processes. Working closely with cross-functional teams, this person will be responsible for implementing quality standards, conducting risk assessments, and driving continuous improvement initiatives to ensure compliance with regulatory requirements and industry best practices.

We are seeking a talented Senior Quality Engineer with medical device experience to ensure that the highest standards of quality and compliance are met for our organization. This position will play a pivotal role in establishing and maintaining robust quality systems and processes to support our first-ever clinical trials through to our manufacturing processes. Working closely with cross-functional teams, this person will be responsible for implementing quality standards, conducting risk assessments, and driving continuous improvement initiatives to ensure compliance with regulatory requirements and industry best practices.