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- Tasks: Create high-quality technical documentation for innovative products in a leading manufacturing company.
- Company: Join a top Lancashire manufacturer with a focus on compliance and quality.
- Benefits: Competitive salary, career growth, and a chance to work in a dynamic environment.
- Why this job: Make a real impact by ensuring product compliance and supporting engineering teams.
- Qualifications: Degree or relevant experience in compliance; knowledge of medical validation is a plus.
- Other info: Collaborative team atmosphere with opportunities for continuous improvement.
The predicted salary is between 36000 - 60000 £ per year.
Jobstore are recruiting on behalf of a leading Lancashire based manufacturer for a Technical Author to be responsible for producing high-quality validation, compliance, and technical documentation to support the design, manufacture, and regulatory assurance of the company’s products. Reporting directly to the Compliance Engineer 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.
What we are looking for:
- Degree qualification or equivalent, or experience in a compliance role in a similar industry.
- Knowledge of medical/pharmaceutical validation requirements is 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.
If this is the new opportunity you are looking for please click to apply now and send your CV for an immediate review.
Technical Author in Rochdale employer: JOBSTORE UK LTD
Contact Detail:
JOBSTORE UK LTD Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Technical Author in Rochdale
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect with professionals on LinkedIn. You never know who might have the inside scoop on job openings or can refer you directly.
✨Tip Number 2
Prepare for interviews by researching the company and its products. Understand their compliance processes and be ready to discuss how your skills align with their needs. Show them you’re not just another candidate!
✨Tip Number 3
Practice your communication skills! As a Technical Author, you'll need to convey complex information clearly. Try explaining technical concepts to friends or family to refine your ability to simplify jargon.
✨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 that extra step to engage with us directly.
We think you need these skills to ace Technical Author in Rochdale
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Technical Author role. Highlight your experience with validation documentation and compliance, as well as any relevant qualifications. We want to see how your skills match what we're looking for!
Showcase Your Attention to Detail: Since this role requires a high level of accuracy, be sure to showcase your attention to detail in your application. Use clear formatting and check for any typos or errors. We appreciate candidates who take pride in their work!
Highlight Team Collaboration: This position involves liaising with various departments, so make sure to mention any experience you have working in teams. We love team players who can communicate effectively across different areas of the business!
Apply Through Our Website: For the best chance of getting noticed, apply through our website. It’s super easy and ensures your application goes directly to us. We can't wait to see what you bring to the table!
How to prepare for a job interview at JOBSTORE UK LTD
✨Know Your Documentation Inside Out
Make sure you’re familiar with the types of documentation mentioned in the job description, like Requirements Traceability Matrices and Operator Manuals. Brush up on your knowledge of validation protocols and compliance standards relevant to the medical and pharmaceutical industries.
✨Showcase Your Teamwork Skills
Since the role involves liaising with various departments, be prepared to discuss examples of how you've successfully collaborated with others in past roles. Highlight your communication skills and how they’ve helped you work effectively in a team setting.
✨Demonstrate Your Attention to Detail
In this role, accuracy is key. Bring examples of your previous work that showcase your meticulousness, especially in producing technical documents. You might even want to mention any tools or methods you use to ensure precision in your work.
✨Stay Updated on Regulations
Familiarise yourself with current regulations and standards that impact the industry. Be ready to discuss how you keep yourself informed about changes in compliance requirements and how you’ve adapted your work accordingly.