Technical Writer

JR United Kingdom; Sheffield; Remote; GBP 50,000 - 60,000; Full time

Job summary

A leading company in medical device regulation is looking for a Technical Writer / Clinical Consultant to join their team. This role offers flexibility with full-time or part-time options, allowing professionals to enhance their skills in a fully remote setting while working on diverse projects. Applicants should have a background in science, engineering, or medicine and a minimum of 2 years in clinical/regulatory experience. Benefits include a competitive salary, company bonus scheme, and health benefits.

Benefits

Company bonus scheme

Health benefits including life insurance

Opportunities for professional growth

Qualifications

• ≥2 years experience in clinical/regulatory roles.
• Knowledge of EU/UK technical documentation and CE/UKCA marking.
• Experience with ISO 13485 and FDA regulations is advantageous.

Responsibilities

• Provide clinical consultancy for medical devices.
• Maintain clinical documentation and conduct technical writing.
• Support clients in regulatory compliance in a remote setting.

Skills

Clinical consultancy

Regulatory compliance

Technical writing

Attention to detail

Communication

Education

Degree or relevant industry experience

Job description

Social network you want to login/join with:

Technical Writer, Sheffield, South Yorkshire

Client:

LFH Regulatory Limited

Location:

Sheffield, South Yorkshire, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

Job Views:

2

Posted:

26.06.2025

Expiry Date:

10.08.2025

Job Description:

Are you an experienced clinical professional looking for a new challenge? LFH Regulatory Limited is seeking a permanent Technical Writer / Clinical Consultant. We are open to full-time or part-time applicants (3 to 5 days).

Benefits include:

• Salary up to £60k pro-rata depending on experience
• Company bonus scheme
• Health benefits including life insurance and critical illness cover

Professional growth: Work on diverse projects, enhance your skills in medical device regulation, and explore opportunities for advancement within our rapidly growing company.

Work environment: Join a team at the forefront of medical device & IVD regulation, contributing to impactful clinical documentation in a fully remote setting with occasional travel.

About LFH Regulatory: We serve clients with diverse technologies, offering a stimulating environment and growth opportunities. Our services include device development, CE/UKCA marking, regulatory strategies, FDA compliance, quality management, audits, and more.

Responsibilities:

• Provide clinical consultancy for medical devices and IVDs
• Support clients in regulatory compliance
• Maintain clinical documentation
• Conduct technical/medical writing, literature reviews, data assessment, and report compilation
• Evaluate clinical and performance data for regulatory submissions
• Create and review documentation such as Clinical Evaluation, Performance Evaluation, Biological Evaluation, etc.

Qualifications:

• Degree or relevant industry experience
• Background in science, engineering, or medicine with clinical/regulatory experience (≥2 years)
• Experience with EU/UK technical documentation and CE/UKCA marking
• US experience is a plus
• Knowledge of ISO 13485 and FDA 21 CFR Part 820
• Team player with good communication skills and attention to detail

Applicants must be based in the UK. Remote work with occasional travel.