Technical Documentation Specialist in Haslingfield

Technical Documentation Specialist in Haslingfield

Haslingfield Full-Time 35000 - 45000 € / year (est.) No home office possible
Hologic

At a Glance

  • Tasks: Create and maintain technical documentation for innovative cancer care products.
  • Company: Join Endomag, a Hologic company, redefining cancer treatment.
  • Benefits: Collaborative culture, personal growth, and the chance to make a real impact.
  • Other info: Dynamic team environment with opportunities for continuous improvement and career advancement.
  • Why this job: Shape the future of cancer care while working with cutting-edge medical technology.
  • Qualifications: Background in engineering or science, with experience in technical documentation.

The predicted salary is between 35000 - 45000 € per year.

Role location: Cambridge, UK

Discover a career with real meaning. One that offers the opportunity to showcase your talents, achieve measurable success and gain immense satisfaction by shaping the future of cancer care.

At Endomag, a Hologic company, we’re redefining cancer treatment and empowering clinicians worldwide with innovative medical solutions. We’re now looking for a Technical Documentation Specialist to join our dynamic team in Cambridge. As a Technical Documentation Specialist, you will play a pivotal role in ensuring the accuracy, consistency and compliance of technical documentation for our products. You will collaborate with multi-disciplinary engineers, clinical trial managers, regulatory affairs specialists and quality assurance experts to create and maintain audit-ready documentation. Your efforts will directly support to deliver innovative, high-quality medical technologies that transform cancer care and improve patient outcomes worldwide.

KEY RESPONSIBILITIES
  • Oversee the creation and maintenance of technical documentation for Endomag’s products, including technical files and design history files, user needs, design inputs, design outputs, verification and validation testing plans and reports, engineering drawings and manufacturing specifications.
  • Lead Cross-Functional Collaboration: act as the primary liaison between R&D, Regulatory Affairs, Clinical Affairs, Product Engineering and Quality Assurance, ensuring seamless integration of their inputs into the technical documentation.
  • Champion Good Documentation Practices: adopt a meticulous approach to creating and editing content, driving efforts to improve documentation practices and ensure consistency and audit readiness.
  • Support Regulatory Compliance: review technical documents to ensure compliance with Endomag’s Quality Management System, FDA, MDR regulations, and applicable international standards (e.g., ISO 13485, ISO 14971).
  • Participate in Regulatory Submissions and Audits: facilitate reviews by internal and external auditors, interact with regulatory agencies as needed, and lead efforts to implement Corrective and Preventive Actions (CAPAs).
KNOWLEDGE, SKILLS & EXPERIENCE
  • Educational background in engineering or a scientific field.
  • Experience in creating and editing technical reports and documentation.
  • Exceptional attention to detail and high levels of accuracy.
  • Demonstrated ability to take ownership of initiatives, deliver results and drive continuous improvement.
  • Excellent content creation and editing skills.
  • Excellent written and verbal communication skills, with the ability to communicate effectively with cross-functional teams and regulatory agencies.
  • Good organizational and time management skills to handle conflicting priorities and meet tight deadlines.
  • Experience in design assurance, quality or technical documentation roles in the medical device industry or other regulated industries, e.g. automotive, aerospace is highly desirable.

Ready to Make an Impact? If you have the right skills and experience and want to join our team, apply today. We can’t wait to hear from you!

Innovate with Purpose: Work at the forefront of life-changing medical technology. Collaborative Culture: Join a friendly, supportive team where your contributions matter. Personal Growth: Expand your skills in a fast-growing, global company.

Technical Documentation Specialist in Haslingfield employer: Hologic

At Endomag, a Hologic company, we pride ourselves on being an exceptional employer that fosters a collaborative culture and prioritises personal growth. Located in the vibrant city of Cambridge, our team is dedicated to redefining cancer care through innovative medical solutions, offering employees the chance to make a meaningful impact while enjoying a supportive work environment and opportunities for professional development.

Hologic

Contact Detail:

Hologic Recruiting Team

StudySmarter Expert Advice🤫

We think this is how you could land Technical Documentation Specialist in Haslingfield

Tip Number 1

Network like a pro! Reach out to folks in the industry, attend meetups or webinars, and connect with people 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 mission and values, especially how they relate to cancer care. This will help you tailor your answers and show that you're genuinely interested in making an impact.

Tip Number 3

Practice your communication skills! As a Technical Documentation Specialist, 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 by the right people. Plus, it shows you’re serious about joining our team at Endomag.

We think you need these skills to ace Technical Documentation Specialist in Haslingfield

Technical Documentation
Cross-Functional Collaboration
Good Documentation Practices
Regulatory Compliance
ISO 13485
ISO 14971
Attention to Detail

Some tips for your application 🫡

Tailor Your CV:Make sure your CV is tailored to the Technical Documentation Specialist role. Highlight relevant experience in creating and editing technical documentation, and don’t forget to showcase your attention to detail and organisational skills!

Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about cancer care and how your skills align with our mission at Endomag. Be sure to mention any experience with regulatory compliance and cross-functional collaboration.

Showcase Your Communication Skills:As a Technical Documentation Specialist, communication is key. In your application, demonstrate your ability to communicate effectively with different teams. Use clear and concise language to reflect your writing skills!

Apply Through Our Website:We encourage you to apply through our website for a smoother process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from our team!

How to prepare for a job interview at Hologic

Know Your Documentation Inside Out

Before the interview, make sure you’re familiar with the types of technical documentation relevant to the role. Brush up on your knowledge of design history files, user needs, and regulatory compliance standards like ISO 13485. This will show that you’re not just interested in the job but also understand the nuances of the documentation process.

Showcase Your Collaboration Skills

Since this role involves working closely with various teams, be prepared to discuss examples of how you've successfully collaborated in the past. Think about specific projects where you acted as a liaison between different departments and how you ensured everyone was on the same page. This will highlight your ability to work in a cross-functional environment.

Demonstrate Attention to Detail

Given the importance of accuracy in technical documentation, be ready to provide examples that showcase your meticulous nature. You might want to mention any processes you’ve implemented to improve documentation practices or how you’ve handled audits in the past. This will reassure them that you can maintain high standards.

Prepare for Regulatory Questions

Expect questions related to regulatory compliance and quality management systems. Familiarise yourself with FDA and MDR regulations, and be ready to discuss how you’ve ensured compliance in previous roles. This will demonstrate your understanding of the industry standards and your readiness to support Endomag’s commitment to quality.