Technical Author-ATEX

Technical Author-ATEX

Full-Time 40000 - 50000 £ / year (est.) No home office possible
ECHELON ENGINEERS

At a Glance

  • Tasks: Create technical documents and ensure compliance for bespoke equipment projects.
  • Company: Established UK manufacturer with a focus on innovation and quality.
  • Benefits: Competitive salary, supportive management, and the chance to build a function from scratch.
  • Other info: Opportunity to develop your skills and grow within a supportive team.
  • Why this job: Be a key player in shaping compliance and quality standards in a dynamic environment.
  • Qualifications: ATEX expertise and direct pharma project experience are essential.

The predicted salary is between 40000 - 50000 £ per year.

A well-established UK manufacturer of bespoke materials handling and process equipment is looking for a Technical Author to own their documentation and compliance function. This is a foundational hire - you will be building the Quality and Compliance function from scratch, with full backing from management to do it properly.

WHAT YOU'LL BE DOING

  • Producing technical files, user manuals, FAT/SAT protocols and regulatory submissions for bespoke equipment projects.
  • Preparing ATEX declarations of conformity and technical files to ATEX Directive 2014/34/EU.
  • Compiling Sistema validation documentation - strategies, protocols, test results and reports.
  • Ensuring compliance across CE marking, PED, machinery directive, ISO standards and pharma GMP requirements.
  • Building the compliance infrastructure from scratch - SOPs, templates, audit trails, document management and working towards ISO 9001.
  • Reporting on quality performance to management and the board.

WHAT WE NEED

  • ATEX expertise is essential - technical files, declarations of conformity, categories and groups.
  • Direct pharma project experience is essential - GMP, cleanroom standards and validation protocols.
  • Sistema validation experience is essential.
  • Strong technical writing skills, a solid grasp of mechanical, electrical and pneumatic systems.

Technical Author-ATEX employer: ECHELON ENGINEERS

Join a well-established UK manufacturer renowned for its bespoke materials handling and process equipment, where you will play a pivotal role in shaping the Quality and Compliance function from the ground up. With a strong commitment to employee development, a collaborative work culture, and the opportunity to make a significant impact, this position offers a rewarding environment for those looking to advance their careers in technical documentation and compliance. Enjoy the backing of management to implement best practices while working in a dynamic sector that values innovation and quality.
ECHELON ENGINEERS

Contact Detail:

ECHELON ENGINEERS Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Technical Author-ATEX

✨Tip Number 1

Network like a pro! Reach out to industry professionals on LinkedIn or attend relevant events. We can’t stress enough how personal connections can open doors that applications alone can’t.

✨Tip Number 2

Prepare for interviews by researching the company and its products. We want you to show genuine interest in their work, especially in areas like ATEX compliance and technical documentation. It’ll set you apart from the crowd!

✨Tip Number 3

Practice your technical writing skills! Since this role involves producing user manuals and technical files, we suggest creating sample documents to showcase your expertise. It’s a great way to demonstrate your skills during interviews.

✨Tip Number 4

Don’t forget to apply through our website! We’ve got all the latest job openings, and applying directly can sometimes give you an edge. Plus, it shows you’re proactive and really interested in joining the team.

We think you need these skills to ace Technical Author-ATEX

Technical Writing Skills
ATEX Expertise
Regulatory Compliance
ISO 9001
GMP Knowledge
Sistema Validation Experience
Document Management
Quality Performance Reporting
Mechanical System Understanding
Electrical System Understanding
Pneumatic System Understanding
Project Management
Attention to Detail
Problem-Solving Skills

Some tips for your application 🫡

Show Off Your ATEX Expertise: Make sure to highlight your experience with ATEX directives and technical files in your application. We want to see how you've tackled similar challenges before, so don’t hold back on the details!

Tailor Your Technical Writing Samples: Include samples of your technical writing that showcase your ability to produce user manuals and compliance documentation. We love seeing how you can make complex information clear and accessible.

Demonstrate Your Compliance Knowledge: Talk about your experience with CE marking, ISO standards, and pharma GMP requirements. We’re building a compliance function from scratch, so your insights here will be super valuable to us!

Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to keep track of your application and ensure it gets the attention it deserves.

How to prepare for a job interview at ECHELON ENGINEERS

✨Know Your ATEX Inside Out

Make sure you brush up on the ATEX Directive 2014/34/EU and understand its implications for technical documentation. Be ready to discuss how you've applied this knowledge in past roles, especially in producing declarations of conformity and technical files.

✨Showcase Your Technical Writing Skills

Prepare examples of your previous work that highlight your technical writing abilities. Bring along samples of user manuals or technical files you've created, and be prepared to explain your process for ensuring clarity and compliance.

✨Demonstrate Your Compliance Knowledge

Familiarise yourself with CE marking, PED, and ISO standards relevant to the role. Be ready to discuss how you've ensured compliance in previous projects and how you would approach building a compliance infrastructure from scratch.

✨Prepare for Scenario Questions

Expect questions that ask you to solve hypothetical problems related to quality and compliance. Think about challenges you've faced in past roles and how you overcame them, particularly in pharma projects and validation protocols.

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