Careers

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In December 2018, InGeneron became one of the first companies to successfully complete a feasibility study as part of the U.S. Food and Drug Administration’s regulatory pathway, using patients’ regenerative cells to treat rotator cuff tendinopathy. Join our fast-growing and leading cell therapy company and shape the future of regenerative medicine. As part of an international team of leading experts with exceptional and diverse backgrounds, you’ll have the opportunity and be challenged to play a pivotal role in translating science to improve patients’ lives.

Here’s What We Value

Co-creating based on respect for and trust in each other.

Seeking input and supporting one another through constructive conversation, coaching and sharing information.

Listening, asking, and challenging the status quo with the belief that open communication stimulates innovation and unleashes the best results.

Prioritizing and focusing on the important aspects your work to become an internal expert.

Getting involved and initiating new ideas that innovate opportunities and head off potential problems.

Showing ownership and accountability. Taking responsibility for your ideas and projects to make sure things get done ethically and on track.

Celebrating success. Thinking bold, working passionately and celebrating your contributions to improving the lives of patients and the care they receive.

Open Positions

We’re a workplace that seeks and draws people who are driven to get better every day. We invite you to explore our open positions below. If you want to keep informed about our development and open positions in the future, please feel free to follow us on LinkedIn, Twitter or Facebook.


Houston, U.S., starting immediately

Regulatory Specialist 

The Regulatory Specialist will coordinate, prepare, or review regulatory submissions for domestic or international projects by preparing regulatory or compliance documentation to local and central IRBs and coordinate/submit regulatory documentation for IRB approval of clinical materials and documents. Additional activities include the review of promotional materials for compliance with applicable regulations and policies in the conduct of clinical research. The candidate must maintain a current knowledge base of existing and emerging regulations, standards, or guidance documents and update this knowledge of legal or regulatory changes to external and internal teams by interpreting regulatory rules or rule changes and ensure that they are communicated through corporate policies and procedures.

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Houston, U.S., starting immediately

Bookkeeper (part-time 20-30 hours per week) 

This position is based at our Houston, TX office. The incumbent will be responsible for maintaining all our vendor accounts in good standing along with processing receipt of payments in a timely fashion. Your responsibilities in this role will support our general accounting department and play a crucial role within our monthly financial operations and month-end close. This position requires a basic understanding of double-entry bookkeeping. The ideal candidate will also have great troubleshooting abilities and attention to detail.

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