Technical Author - Medical Devices & Regulatory Documentation

Rise Technical; Bury St Edmunds; On-site; GBP 40,000 - 45,000; Full time

Job summary

A healthcare solutions provider is seeking a Technical Author to produce essential validation and technical documentation within the medical devices sector. This role involves creating manuals, test protocols, and regulatory submissions to support crucial healthcare products. Ideal candidates should have a degree in a technical field and knowledge of industry regulations such as CE and UKCA compliance. The position offers opportunities for professional development and is well-suited for individuals looking to make a meaningful impact in healthcare.

Benefits

Bonus

Life Assurance

Excellent Company Benefits

Qualifications

• Degree-qualified or equivalent experience in a technical or compliance role.
• Knowledge of CE, UKCA compliance, and related directives is desirable.
• Looking for training and career development.

Responsibilities

• Prepare and maintain validation and compliance documentation.
• Produce Standard Test Protocols and procedure manuals.
• Monitor, interpret, and report on relevant regulations.

Skills

Attention to detail

Technical documentation expertise

Collaboration skills

Education

Degree in a relevant technical field

Job description

A healthcare solutions provider is seeking a Technical Author to produce essential validation and technical documentation within the medical devices sector. This role involves creating manuals, test protocols, and regulatory submissions to support crucial healthcare products. Ideal candidates should have a degree in a technical field and knowledge of industry regulations such as CE and UKCA compliance. The position offers opportunities for professional development and is well-suited for individuals looking to make a meaningful impact in healthcare.