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For Companies At a Glance
- Tasks: Create high-quality technical documentation and collaborate with various teams.
- Company: Join Envair Technology, a leader in clean air solutions for healthcare.
- 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 40000 - 45000 £ 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 employer: Envair Limited
Contact Detail:
Envair Limited Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Technical Author
✨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 apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who take the initiative to engage directly with us.
We think you need these skills to ace Technical Author
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!
Showcase Your Attention to Detail: As a Technical Author, accuracy is key! Use clear formatting and check for typos or errors in your application. We love candidates who take pride in their work.
Be Proactive in Your Cover Letter: Use your cover letter to explain why you’re the perfect fit for us. Share specific examples of your past work that align with our mission and values. We want to see your passion!
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 don’t miss out on any important updates from us!
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 terms like FAT, IQOQ, and risk assessments. This will show that you're not just a candidate, but someone who understands the industry.
✨Showcase Your Documentation Skills
Prepare examples of high-quality technical documentation you've produced in the past. Whether it's operator manuals or compliance documents, having tangible examples will demonstrate your capability and attention to detail.
✨Be a Team Player
Since collaboration is key in this role, be ready to discuss how you've worked with different departments in previous jobs. Share specific instances where your communication skills helped bridge gaps between teams.
✨Stay Updated on Regulations
Research current regulations and standards relevant to the role. Being able to discuss recent changes and their implications shows that you're proactive and committed to continuous improvement, which aligns perfectly with the company's values.
