Open Positions

Help us innovate in a rewarding line of work
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We are an innovative and fast-paced team advancing a diverse array of therapeutics

With Theradaptive, you will experience the challenge and satisfaction of the therapeutic product development process firsthand. Transform your career and join the Theradaptive team today!

Theradaptive offers a comprehensive benefits package that includes:
Scientist I, Analytical Development

We are seeking a talented Analytical Development Scientist I to join our team. The ideal candidate will play a key role in developing, troubleshooting, and conducting assays using chromatography, electrophoresis, and immunoassay techniques. These assays are crucial in supporting the development, manufacturing, and characterization of Biologic Drug Substances and Drug Product/Medical Devices. The candidate will be expected to make detailed experimental observations, analyzing data, interpreting experimental results, and summarizing findings for presentations and reports. Additionally, the successful candidate will have the opportunity to contribute to the authoring and revision of SOPs, protocols, technical reports, and other relevant documentation.

Senior Quality Engineer (Japanese/English Bilingual)

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.

Senior Quality Engineer (Medical Devices)

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.

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