Technical Author in London

Technical Author in London

London Full-Time 34000 - 51000 £ / year (est.) No home office possible
Go Premium
E

At a Glance

  • Tasks: Create high-quality technical documentation and collaborate with various teams.
  • Company: Join Envair Technology, a leader in clean air solutions since 1972.
  • Benefits: Competitive salary, annual bonus, health cash plan, and nursery vouchers.
  • Why this job: Make a real impact in healthcare by supporting vital projects.
  • Qualifications: Degree or experience in compliance, with strong communication skills.
  • Other info: Dynamic workplace with a commitment to diversity and career growth.

The predicted salary is between 34000 - 51000 £ per year.

We are currently looking for a Technical Author to join our growing team in Heywood on a permanent contract. As a Technical Author, you will be part of a team in our long-established business, delivering projects and developing market leading solutions that benefit our extensive client base. This is a full-time and permanent role.

The Benefits

  • Annual salary £40,000 – 45,000
  • Annual bonus based on company performance
  • Simply Health cash back plan
  • Credit Union
  • Nursery voucher salary sacrifice scheme

Location

Our clean, bright 63,000 sq. ft. site in Heywood, Lancashire is the largest containment factory in the North West, just minutes from the M66 and M62. We have invested £1m in our facility, with state-of-the-art machinery and excellent staff facilities including showers, canteen and plenty of on-site parking.

About us

Envair Technology have been manufacturing world class clean air and containment equipment for the healthcare and pharmaceutical industries since 1972. Our mission is to engineer controlled environments that keep people and products safe from airborne hazards. Our products, including isolators, laminar airflow cabinets and microbiological safety cabinets, are used to prepare chemotherapy treatments for cancer patients, discover new therapies for Alzheimer’s or test samples in hospitals. It means you’ll always finish the day feeling you’ve contributed to something really valuable, supporting our NHS and private hospitals throughout Europe.

We’ve enjoyed strong growth in demand for our products for the last few years, and as industry leaders, are always looking to bring new innovations to the market. It’s why we look for people who share our values of taking pride in your work, being ambitious and inventive, nurturing the people around you and collaborating as a team.

Your Role

As our Technical Author, you will work for the Compliance Engineer and be responsible for producing high-quality validation, compliance, and technical documentation to support the design, manufacture, and regulatory assurance of the company’s products. You will:

  • Prepare the required validation documentation including the Requirements Traceability Matrices, Design Qualifications, Factory Acceptance Tests, Installation and Operation Qualifications, Operator Manuals, Risk Assessment and Method Statements.
  • Produce Standard Test Protocols and procedure manuals.
  • Work closely with the Compliance Engineer to scope out and implement continuous improvement in the production and management of validation documentation.
  • Liaise directly with other areas of the business such as the Production, Customer Care, Sales, and After Market departments on behalf of the Engineering Team.
  • Work according to the applicable protocols, guidelines and legal standards as required.
  • Work with our customers to understand their requirements and respond to their requests for compliance information.
  • Monitor and report on new and updated regulations and standards and their impacts on the company’s products.

About You

We are looking for someone with the following attributes:

  • A degree qualification or equivalent, or experience in a compliance role in a similar industry
  • Knowledge of medical/pharmaceutical validation requirements (desirable)
  • A proven track record in the development and execution of validation protocols such as risk assessments, design qualifications, FAT, IQOQ, and Operator Manuals or similar
  • Working knowledge of CE, UKCA compliance and any associated directives; including but not limited to Low Voltage, EMF, and ATEX
  • Experience working under GMP (desirable but not essential)
  • Strong team player with excellent communication skills, both written and verbal
  • High attention to detail and commitment to accuracy
  • Proactive, analytical, and able to work with minimal supervision
  • Comfortable working within regulated environments

Envair Technology are an equal opportunities employer. We value diversity and are strongly committed to providing equal employment opportunities for all employees and all applicants for employment. Equal opportunities are the only acceptable way to conduct business and we believe that the more inclusive our environments are, the better our work will be.

Apply for this job

If you can see yourself in this position, send us your CV using the form below. If we think you have the talents we’re looking for, we’ll be in touch within 10 working days.

Technical Author in London employer: Envair Limited

Envair Technology is an exceptional employer, offering a dynamic work environment in Heywood where innovation meets purpose. With a commitment to employee growth, competitive salaries, and comprehensive benefits including a cash back health plan and nursery vouchers, we foster a culture of collaboration and pride in our work. Join us in making a meaningful impact on healthcare while enjoying state-of-the-art facilities and a supportive team atmosphere.
E

Contact Detail:

Envair Limited Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Technical Author in London

✨Tip Number 1

Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.

✨Tip Number 2

Prepare for interviews by researching the company and its products. Understand their mission and values, especially how they relate to healthcare and pharmaceutical industries. This will help you show that you're genuinely interested in being part of their team.

✨Tip Number 3

Practice your responses to common interview questions, but keep it natural. Use the STAR method (Situation, Task, Action, Result) to structure your answers, especially when discussing your experience with compliance and technical documentation.

✨Tip Number 4

Don’t forget to follow up after your interview! A simple thank-you email can go a long way in showing your enthusiasm for the role. And remember, apply through our website for the best chance at landing that Technical Author position!

We think you need these skills to ace Technical Author in London

Technical Documentation
Validation Protocols
Compliance Knowledge
Risk Assessment
Design Qualifications
Factory Acceptance Tests (FAT)
Installation and Operation Qualifications (IQOQ)
Operator Manuals
CE Compliance
UKCA Compliance
GMP Knowledge
Communication Skills
Attention to Detail
Analytical Skills
Team Collaboration

Some tips for your application 🫡

Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Technical Author role. Highlight any relevant experience in compliance and technical documentation to catch our eye!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about the role and how your background aligns with our mission at Envair Technology. Keep it concise but impactful.

Showcase Your Attention to Detail: As a Technical Author, precision is key. Ensure your application is free from typos and errors. This not only shows your attention to detail but also your commitment to quality work.

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!

How to prepare for a job interview at Envair Limited

✨Know Your Stuff

Make sure you brush up on your knowledge of medical and pharmaceutical validation requirements. Familiarise yourself with key documents like Design Qualifications and Operator Manuals, as well as compliance standards like CE and UKCA. This will show that you're not just a good fit for the role, but that you genuinely understand the industry.

✨Showcase Your Experience

Prepare to discuss your previous experience in developing validation protocols and working under GMP. Have specific examples ready that highlight your attention to detail and ability to work independently. This will help demonstrate your capability to handle the responsibilities of the Technical Author position.

✨Communicate Clearly

As a Technical Author, communication is key. Practice explaining complex technical concepts in simple terms. During the interview, be clear and concise in your responses, and don’t hesitate to ask for clarification if you don’t understand a question. This shows that you value effective communication.

✨Emphasise Teamwork

Since the role involves liaising with various departments, be prepared to discuss how you’ve successfully collaborated with others in the past. Share examples of how you’ve worked as part of a team to achieve common goals, and express your enthusiasm for contributing to a collaborative environment at Envair Technology.

Technical Author in London
Envair Limited
Location: London
Go Premium

Land your dream job quicker with Premium

You’re marked as a top applicant with our partner companies
Individual CV and cover letter feedback including tailoring to specific job roles
Be among the first applications for new jobs with our AI application
1:1 support and career advice from our career coaches
Go Premium

Money-back if you don't land a job in 6-months

E
Similar positions in other companies
UK’s top job board for Gen Z
discover-jobs-cta
Discover now
>