At a Glance
- Tasks: Create and maintain technical documentation for innovative cancer care products.
- Company: Join Endomag, a Hologic company, redefining cancer treatment.
- Benefits: Competitive salary, career growth, and the chance to make a real impact.
- Other info: Collaborate with diverse teams in a dynamic environment.
- Why this job: Shape the future of cancer care and improve patient outcomes worldwide.
- Qualifications: Background in engineering or science with strong writing skills.
The predicted salary is between 40000 - 50000 € per year.
Role location: 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 are redefining cancer treatment and empowering clinicians worldwide with innovative medical solutions. We are 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.
- 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.
- 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.
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.
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.
Work at the forefront of life-changing medical technology.
Technical Writer/Editor (Full Time) in Cambridge employer: Hologic
At Endomag, a Hologic company, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture in the heart of Cambridge. Our commitment to employee growth is evident through continuous learning opportunities and the chance to contribute to groundbreaking advancements in cancer care, making your role as a Technical Documentation Specialist not just a job, but a meaningful career that impacts lives globally.
StudySmarter Expert Advice🤫
We think this is how you could land Technical Writer/Editor (Full Time) in Cambridge
✨Tip Number 1
Network like a pro! Reach out to folks in the medical tech industry, especially those at Endomag. A friendly chat can open doors and give you insights that job descriptions just can't.
✨Tip Number 2
Showcase your skills! Create a portfolio of your technical documentation work. This is your chance to shine and demonstrate how you can contribute to Endomag's mission of transforming cancer care.
✨Tip Number 3
Prepare for interviews by brushing up on regulatory compliance and good documentation practices. Be ready to discuss how your experience aligns with Endomag's needs and how you can help maintain audit-ready documentation.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take that extra step to connect with us directly.
We think you need these skills to ace Technical Writer/Editor (Full Time) in Cambridge
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Technical Writer/Editor role. Highlight your experience in creating and editing technical documentation, especially in regulated industries like medical devices. We want to see how your skills align with our mission at Endomag!
Showcase Your Collaboration Skills:Since you'll be working closely with various teams, emphasise your ability to collaborate effectively. Share examples of how you've liaised with engineers, regulatory affairs, or quality assurance teams in your previous roles. We love a team player!
Demonstrate Attention to Detail:Good documentation practices are key for us. In your application, mention specific instances where your meticulous approach has improved documentation quality or compliance. This will show us you're serious about maintaining high standards.
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 don’t miss any important updates. Plus, we love seeing applications come in through our own platform!
How to prepare for a job interview at Hologic
✨Know Your Stuff
Make sure you brush up on the technical aspects of the role. Familiarise yourself with the types of documentation you'll be working on, like design history files and verification plans. Being able to discuss these confidently will show that you're serious about the position.
✨Showcase Your Collaboration Skills
Since this role involves working with various teams, think of examples where you've successfully collaborated in the past. Be ready to share how you’ve liaised with different departments, like R&D or Quality Assurance, to create comprehensive documentation.
✨Emphasise Attention to Detail
This job requires a meticulous approach to documentation. Prepare to discuss your methods for ensuring accuracy and compliance in your work. You might even want to bring along samples of your previous documentation to highlight your skills.
✨Understand Regulatory Standards
Familiarise yourself with relevant regulations like FDA and MDR. Be prepared to discuss how you’ve ensured compliance in your previous roles. This knowledge will demonstrate your readiness to support regulatory submissions and audits effectively.
