Technical Author / Medical Devices

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

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'll 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 organisation is an industry leader in controlled environment solutions and have invested heavily in state-of-the-art facilities and machinery to support its teams. You'll benefit from a collaborative environment where innovation, accuracy, and quality are valued.

If you are looking for a role where your work genuinely makes a difference while offering structured development and a supportive culture, this position provides an ideal platform to grow your career.

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

Rise Technical Recruitment Ltd acts an employment agency for permanent roles and an employment business for temporary roles.

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