At MINUS150, we’re on a mission to make advanced cryogenic monitoring accessible, dependable, and impactful. We work with leading conservation organisations and non-profits to protect endangered species and safeguard irreplaceable biological materials.
While conservation remains our core focus, our technology also supports a wide range of applications — from veterinary care and breeding programs to livestock management, logistics, and warehousing.
As we expand our platform, we’re also exploring the transition into human biostorage — applying the same principles of precision and safety to new, medically-adjacent fields. Our mission-driven approach ensures that everything we build drives real, measurable change in the world.
Role Description:
We’re looking for a Quality and Regulatory Advisor to support our growing operations and ensure compliance as we move toward medical device-grade standards. This is a part-time, on-site role based in the UK.
You’ll play a key role in helping us maintain the highest levels of quality, safety, and compliance, initially focused on our conservation and veterinary solutions - with a view toward future expansion into human biostorage and medical applications.
Responsibilities:
* Managing and interpreting regulatory frameworks
* Ensuring ongoing compliance with standards such as ISO 13485, ISO 14971, and IEC 62304
* Developing and maintaining documentation to support quality management systems (QMS)
* Preparing regulatory submissions and audit documentation
* Conducting internal quality audits and risk assessments
* Advising the team on emerging regulations, compliance issues, and best practices
Qualifications:
* Strong knowledge of medical device regulations and quality management systems
* Proficiency with ISO 13485 and related standards (e.g., ISO14971, IEC62304, EU MDR, FDA 21 CFR Part 820)
* Demonstrated experience in regulatory affairs and compliance documentation
* Excellent analytical, communication, and interpersonal skills
* Detail-oriented with strong organizational abilities and the capacity to work independently
* Bachelor's degree in Regulatory Affairs, Quality Management, Biomedical Engineering, or a related field
* Experience in cryogenic systems, life sciences, or medical devices is highly desirable
Seniority level
Entry level
Employment type
Contract
Job function
Legal
Industries
Technology, Information and Internet
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