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- 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 impactful work.
- Why this job: Make a real difference in cancer care while developing your skills.
- Qualifications: Background in engineering or science, with strong documentation skills.
- Other info: Dynamic team environment with a focus on continuous improvement.
The predicted salary is between 28800 - 48000 ÂŁ per year.
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 the delivery of 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).
- 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 Cambridge employer: Hologic, Inc.
Contact Detail:
Hologic, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Technical Documentation Specialist in Cambridge
✨Tip Number 1
Network like a pro! Reach out to folks in the industry, attend relevant events, and connect with people 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 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 and contributing to innovative cancer care solutions.
We think you need these skills to ace Technical Documentation Specialist in Cambridge
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Technical Documentation Specialist role. Highlight your experience in creating technical documentation and any relevant regulatory knowledge, as this will show us you understand what we're looking for.
Showcase Your Attention to Detail: Since accuracy is key in this role, give examples of how you've maintained high standards in your previous work. We want to see that you can produce audit-ready documentation without a hitch!
Highlight Collaboration Skills: We love teamwork at StudySmarter! Mention any experiences where you've worked with cross-functional teams, especially in regulated environments. This will demonstrate your ability to liaise effectively with various stakeholders.
Apply Through Our Website: Don't forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role. We can’t wait to see what you bring to the table!
How to prepare for a job interview at Hologic, Inc.
✨Know Your Stuff
Make sure you’re well-versed in the technical aspects of documentation relevant to the medical device industry. Brush up on regulations like ISO 13485 and MDR, as well as good documentation practices. This will show that you’re not just familiar with the role but also passionate about compliance and quality.
✨Showcase Your Collaboration Skills
Since this role involves working with various teams, be prepared to discuss your experience in cross-functional collaboration. Think of specific examples where you’ve successfully liaised between different departments, like R&D and Quality Assurance, to create comprehensive documentation.
✨Attention to Detail is Key
Highlight your meticulous nature during the interview. Bring examples of how your attention to detail has positively impacted previous projects, especially in creating or editing technical documents. This will demonstrate your ability to maintain high standards in documentation.
✨Prepare for Regulatory Questions
Expect questions about your experience with regulatory submissions and audits. Be ready to discuss how you’ve handled compliance issues in the past and your approach to implementing corrective actions. This will show that you understand the importance of regulatory frameworks in the medical field.