Technical Author / Medical Devices

Rise Technical Recruitment; Limefield; On-site; GBP 40,000 - 45,000; Full time

Job summary

A healthcare engineering firm based in Limefield is seeking a meticulous Technical Author to produce critical documentation like validation and compliance reports. This role involves preparing manuals and test protocols that ensure products meet industry regulations, crucial for supporting safe patient and laboratory environments. The ideal candidate will hold a technical degree and have knowledge of medical or regulated industries, with opportunities for professional growth and skills enhancement. Competitive salary and benefits package offered.

Benefits

Bonus

Life Assurance

Excellent Company Benefits

Qualifications

• Degree-qualified or equivalent in a technical or compliance role, preferable in medical or regulated industries.
• Knowledge of CE, UKCA compliance and 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

Regulatory compliance knowledge

Technical documentation expertise

Education

Degree in a technical or compliance field

Job description

Technical Author (Medical Devices / Engineering)

Bury, commutable from: Manchester, Rochdale, Oldham, Failsworth, Bolton, Heywood, Farnworth, Middleton, Prestwich, Ramsbottom, Littleborough & all surrounding areas

£40,000 - £45,000 + Bonus + Life Assurance + Excellent Company Benefits

Are you a meticulous Technical Author or documentation professional looking to make an impact in the healthcare and pharmaceutical engineering sector?

You will be responsible for producing validation, compliance, and technical documentation, including operator manuals, test protocols, risk assessments, and regulatory submissions. Your work will directly support products that keep patients and laboratory environments safe, giving your role a real sense of purpose.

This is a chance to join a growing, innovative business delivering world-class containment and clean air equipment, giving you exposure to regulatory compliance, product validation and cross‑departmental collaboration, alongside opportunities for professional development and skills progression.

The Role

• Prepare and maintain validation and compliance documentation.
• Produce Standard Test Protocols and procedure manuals to support the design and manufacture of products.
• Monitor, interpret, and report on relevant regulations and standards impacting products.

The Candidate

• Degree-qualified or equivalent experience in a technical or compliance role, ideally within medical, pharmaceutical, or regulated industries.
• Knowledge of CE, UKCA compliance and related directives (Low Voltage, EMF, ATEX) desirable.
• Looking for training and career development.

We are an equal opportunities company and welcome applications from all suitable candidates.