We are seeking a creative and detail-oriented Documentation Specialist with a passion for medical technology, and will consider both part-time and full-time support. The position is ideal for someone currently working in or aspiring to transition into regulatory affairs. The selected candidate will play a vital role in helping us advance our product offering to the next level of production and clinical support, and will be involved in all aspects of design verification and validation, working closely with our engineering and regulatory team.

Full-time remote candidates will be considered, but the ideal candidate will be located in the greater Charlotte, NC area.