Technical Documentation Specialist in Hartford

Technical Documentation Specialist in Hartford

Hartford 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 opportunities, and meaningful work.
  • Other info: Dynamic team environment with a focus on continuous improvement.
  • Why this job: Make a real impact in life-changing medical technology.
  • Qualifications: Background in engineering or science with technical documentation experience.

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 Hartford 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. With opportunities for skill expansion and a commitment to excellence, joining us as a Technical Documentation Specialist means becoming part of a mission-driven organisation that values your contributions and encourages continuous improvement.

Hologic

Contact Detail:

Hologic Recruiting Team

StudySmarter Expert Advice🤫

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

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’re transforming cancer care. This will help you tailor your answers and show you’re genuinely interested.

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. Plus, we love seeing candidates who are proactive about joining our team at Endomag.

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

Technical Documentation
Attention to Detail
Regulatory Compliance
Good Documentation Practices
Cross-Functional Collaboration
Content Creation and Editing
Communication Skills

Some tips for your application 🫡

Tailor Your CV:Make sure your CV reflects the skills and experiences that align with the Technical Documentation Specialist role. Highlight any relevant experience in creating technical documentation, especially in regulated industries like medical devices.

Craft a Compelling Cover Letter:Use your cover letter to tell us why you're passionate about cancer care and how your background makes you a great fit for our team. Be specific about your experience with cross-functional collaboration and good documentation practices.

Showcase Your Attention to Detail:In your application, demonstrate your meticulous approach to documentation. Mention any specific examples where your attention to detail made a difference in your previous roles, especially in compliance or quality assurance.

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 shows us you’re keen on joining our innovative team!

How to prepare for a job interview at Hologic

Know Your Stuff

Make sure you brush up on the technical aspects of documentation relevant to the medical device industry. Familiarise yourself with standards like ISO 13485 and ISO 14971, as well as the specific regulations that Endomag adheres to. This will show your potential employer that you're not just interested in the role, but that you understand the industry's requirements.

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 highlight how your communication skills helped achieve a common goal.

Attention to Detail is Key

Given the importance of accuracy in technical documentation, be ready to demonstrate your meticulous approach. You might want to bring along samples of your previous work or discuss how you ensure consistency and compliance in your documentation practices. This will help illustrate your commitment to quality.

Prepare for Regulatory Questions

Expect questions related to regulatory compliance and audits. Brush up on your knowledge of the FDA and MDR regulations, and think about how you've handled similar situations in the past. Being able to articulate your experience with regulatory submissions will set you apart from other candidates.