Clinical Affairs Associate

at  Bedfont scientific

THE CHALLENGE:

Healthcare is evolving and the market for breath analysis monitors is expanding. Bedfont are looking for
hard-working, like-minded, and passionate individuals to join the Bedfont Family to help achieve its goal
of innovating healthcare worldwide.

QUALIFICATIONS:

A bachelor’s degree in Biomedical Science, life sciences, another related field or equivalent experience
would be preferred. A qualification in medical writing and/or technical writing is preferred, but not

essential. The following experience would also be advantageous:

• Previous experience in medical and technical writing.
• Previous experience in supporting PMS, PCMF, risk management, and clinical evaluation

activities.

• Familiarity with regulatory requirements and guidance documents for medical devices, such as

FDA regulations (e.g., 510(k), PMA) and international standards (e.g., ISO 13485, EU MDR,

PREFERRED SKILLS:

• Strong Communication Skills: Ability to convey information clearly, both in writing and verbally,

to team members and consultants.

• Attention to Detail: Meticulous in reviewing data, documentation, and regulatory requirements.
• Organisational Skills: Capable of managing multiple tasks, projects, and timelines effectively.
• Adaptability: Thrives in a fast-paced environment with shifting priorities.
• Regulatory Compliance Awareness: Understanding of global regulatory landscapes, including

EU, US, and international standards.

• Self-Motivation: Works independently with minimal supervision to meet goals.