Medical Device Technical Author – Regulatory & Validation

Rise Technical Recruitment; Limefield; On-site; GBP 80,000 - 100,000; Full time

Job summary

A healthcare engineering firm is seeking a meticulous Technical Author to produce critical documentation such as validation and compliance reports. This role involves preparing manuals and test protocols that ensure products meet industry regulations. The ideal candidate should hold a technical degree and possess knowledge of medical or regulated industries, offering opportunities for professional growth and skill enhancement. A competitive salary and benefits package are offered.

Benefits

Competitive salary

Benefits package

Professional growth opportunities

Qualifications

• Must have a technical degree relevant to healthcare engineering.
• Experience in producing validation and compliance documentation is preferred.
• Knowledge of industry regulations for medical products is critical.

Responsibilities

• Produce critical documentation including validation and compliance reports.
• Prepare manuals and test protocols ensuring regulations are met.
• Support safe patient and laboratory environments through documentation.

Skills

Meticulous attention to detail

Knowledge of medical or regulated industries

Technical writing skills

Education

Technical degree

Job description

A healthcare engineering firm is seeking a meticulous Technical Author to produce critical documentation such as validation and compliance reports. This role involves preparing manuals and test protocols that ensure products meet industry regulations. The ideal candidate should hold a technical degree and possess knowledge of medical or regulated industries, offering opportunities for professional growth and skill enhancement. A competitive salary and benefits package are offered.