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- Tasks: Create and revise technical documents for innovative medical device projects.
- Company: Join a leading team in the biomedical engineering field.
- Benefits: Gain valuable experience in a regulated industry with potential for growth.
- Why this job: Make a difference in healthcare by contributing to essential regulatory submissions.
- Qualifications: Bachelor’s degree and strong writing skills required; experience in medical devices preferred.
- Other info: Collaborative environment with opportunities to work alongside experts in the field.
The predicted salary is between 36000 - 60000 £ per year.
The Technical Writer will support the Client Preclinical Engineering team with the creation, revision and proofreading of reports and technical content for bench and in vivo testing. These documents will be leveraged in regulatory submissions and will require specific compliance to formatting and content specifications.
Responsibilities:
- Collaboration with Research & Development teams, including subject matter experts on Preclinical Engineering, Hardware and Ablation Catheter Design teams.
- Coordinating document approval process according to team procedural requirements.
- With limited supervision, drafting reports and technical content in the context of bench and in vivo preclinical studies.
Required Qualifications:
- Bachelor’s degree, with at least three years of relevant experience, preferably within the medical device or biomedical engineering fields.
Preferred Qualifications:
- Bachelor’s degree in communications, engineering, technical writing or within the realm of the physical or biological sciences.
- Experience within a regulated industry (e.g., medical devices).
- Strong writing, editing and communication skills.
- Able to balance efficient authoring and editing of documents while maintaining a high standard in quality of work.
- Proficiency in Microsoft Word and Excel.
Technical Writer in Plymouth employer: LanceSoft Inc
Contact Detail:
LanceSoft Inc Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Technical Writer in Plymouth
✨Tip Number 1
Network like a pro! Reach out to folks in the medical device or biomedical engineering fields. Use LinkedIn to connect with professionals and join relevant groups. You never know who might have the inside scoop on job openings!
✨Tip Number 2
Prepare for interviews by brushing up on your technical writing skills. Be ready to discuss your experience with regulatory submissions and document formatting. Practice explaining complex concepts in simple terms – it’s a key skill for a Technical Writer!
✨Tip Number 3
Showcase your portfolio! Have samples of your previous work ready to share during interviews. Highlight documents that demonstrate your ability to create clear, compliant reports, especially in regulated industries.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities waiting for you. Plus, applying directly can sometimes give you an edge over other candidates. Let’s get you that Technical Writer role!
We think you need these skills to ace Technical Writer in Plymouth
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Technical Writer role. Highlight your experience in technical writing, especially in regulated industries like medical devices. We want to see how your skills match what we're looking for!
Showcase Your Writing Skills: Include samples of your writing or links to your portfolio. This is your chance to show us your strong writing and editing skills. Remember, clarity and precision are key in technical writing!
Follow the Format: Pay attention to the formatting requirements in the job description. We appreciate candidates who can follow guidelines, as this reflects your ability to adhere to compliance standards in your work.
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep everything organised and ensures your application gets the attention it deserves!
How to prepare for a job interview at LanceSoft Inc
✨Know Your Stuff
Make sure you brush up on the technical aspects of the role. Familiarise yourself with the specifics of preclinical studies and the medical device industry. This will help you speak confidently about your experience and how it relates to the job.
✨Showcase Your Writing Skills
Prepare samples of your previous work that highlight your writing, editing, and communication skills. Be ready to discuss how you approach drafting and revising technical documents, especially in a regulated environment.
✨Understand the Approval Process
Get a good grasp of document approval processes in regulated industries. Be prepared to discuss how you’ve navigated similar processes in the past and how you ensure compliance with formatting and content specifications.
✨Ask Smart Questions
Prepare thoughtful questions about the team dynamics, collaboration with R&D, and the specific challenges they face. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
