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For Companies At a Glance
- Tasks: Create vital documentation for medical devices that ensure safety and compliance.
- Company: Join a leading company in healthcare engineering with a focus on innovation.
- Benefits: Enjoy a competitive salary, bonuses, life assurance, and excellent perks.
- Why this job: Make a real difference in healthcare while developing your skills in a supportive environment.
- Qualifications: Degree or equivalent experience in a technical role, preferably in regulated industries.
- Other info: Collaborative culture with opportunities for professional growth and development.
The predicted salary is between 28800 - 36000 £ per year.
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 organisation is an industry leader in controlled environment solutions and has invested heavily in state-of-the-art facilities and machinery to support its teams. You will 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.
Technical Author (Medical Devices / Engineering) in Bury St Edmunds employer: Rise Technical
Contact Detail:
Rise Technical Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Technical Author (Medical Devices / Engineering) in Bury St Edmunds
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical devices and engineering sectors on LinkedIn. Join relevant groups, participate in discussions, and don’t be shy about asking for informational interviews. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for those interviews by researching the company inside out. Understand their products, values, and recent news. We want you to show them that you’re not just another candidate; you’re genuinely interested in making an impact in their team!
✨Tip Number 3
Practice your technical explanations! As a Technical Author, you’ll need to convey complex information clearly. We suggest doing mock interviews with friends or mentors to refine your communication skills and ensure you can articulate your expertise effectively.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to engage directly with us. Let’s get you that dream job together!
We think you need these skills to ace Technical Author (Medical Devices / Engineering) in Bury St Edmunds
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Technical Author role. Highlight your experience in producing technical documentation, especially in medical devices or engineering. We want to see how your skills align with our needs!
Showcase Relevant Experience: When writing your application, focus on your experience with compliance and validation documentation. Mention any specific projects or roles where you’ve worked with regulations like CE or UKCA. This will help us see your fit for the position.
Be Clear and Concise: In your written application, clarity is key! Use straightforward language and avoid jargon unless it’s relevant. We appreciate a well-structured application that gets straight to the point, showcasing your qualifications effectively.
Apply Through Our Website: We encourage you to apply through our website for the best chance of getting noticed. It’s super easy and ensures your application goes directly to us. Plus, we love seeing candidates who take the initiative to connect with us directly!
How to prepare for a job interview at Rise Technical
✨Know Your Stuff
Make sure you brush up on the technical aspects of medical devices and compliance regulations. Familiarise yourself with CE and UKCA compliance, as well as any relevant directives. This will show that you're not just a candidate, but someone who understands the industry.
✨Showcase Your Documentation Skills
Prepare examples of your previous work, especially any validation or compliance documentation you've created. Be ready to discuss how you approach writing operator manuals or test protocols, as this is crucial for the role.
✨Understand the Company Culture
Research the company’s values and recent projects. Knowing about their focus on innovation and quality will help you align your answers with what they’re looking for. It also shows genuine interest in the role and the organisation.
✨Ask Insightful Questions
Prepare thoughtful questions about the team dynamics, professional development opportunities, and how they measure success in the role. This not only demonstrates your enthusiasm but also helps you gauge if the company is the right fit for you.
