What are the responsibilities and job description for the Sr. Technical Writer (Medical Device, HW/SW, MadCap Flare) position at Leica Biosystems?
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Leica Biosystems, one of Danaher’s 15 operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
At Leica Biosystems, we’re not just shaping the future of cancer diagnostics — we’re transforming lives. Our mission of “Advancing Cancer Diagnostics, Improving Lives” is the driving force behind everything we do. As a global leader with the most comprehensive portfolio spanning from biopsy to diagnosis, we empower clinicians with innovative, reliable solutions so they can give patients timely, accurate answers when they need them most. When you join Leica Biosystems, you’re not just taking a job; you’re becoming part of a passionate team that knows every moment matters when it comes to cancer. You’ll help develop diagnostic solutions that turn anxiety into answers, and aid the acceleration of next-generation, life-changing therapies. Surrounded by a diverse and collaborative global community, you’ll be inspired each day to stretch, grow, and make an impact.
Learn about the Danaher Business System which makes everything possible.
The Senior Technical Writer for Leica Biosystems creates accurate, compliant technical documentation for our Digital Pathology portfolio. Focused on internal and external customer needs, this role develops and maintains user guides, service manuals, and technical instructions that enable the safe, efficient installation, operation, and support of our products. You will collaborate closely with R&D, Quality, Regulatory, and Service & Support stakeholders to translate complex technical data into clear, usable content throughout the product lifecycle. Additionally, this role ensures all materials remain current with strict regulatory and business requirements. This position reports to the Manager, Technical Writing & Training, and is an onsite role based in the Digital Pathology Business Unit in Vista, CA.
This position reports to the Manager, Technical Writing & Training and is part of the Technical Publications Training Team located onsite in the Digital Pathology Business Unit in Vista, CA.
In This Role, You Will Have The Opportunity To
Ability to travel <10% domestically or internationally
It would be a plus if you also possess previous experience in:
The annual salary range for this role is $100,000 - $115,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.
#thisisbelonging
#thebestteamisdiverse
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
The U.S. EEO posters are available here.
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Leica Biosystems, one of Danaher’s 15 operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
At Leica Biosystems, we’re not just shaping the future of cancer diagnostics — we’re transforming lives. Our mission of “Advancing Cancer Diagnostics, Improving Lives” is the driving force behind everything we do. As a global leader with the most comprehensive portfolio spanning from biopsy to diagnosis, we empower clinicians with innovative, reliable solutions so they can give patients timely, accurate answers when they need them most. When you join Leica Biosystems, you’re not just taking a job; you’re becoming part of a passionate team that knows every moment matters when it comes to cancer. You’ll help develop diagnostic solutions that turn anxiety into answers, and aid the acceleration of next-generation, life-changing therapies. Surrounded by a diverse and collaborative global community, you’ll be inspired each day to stretch, grow, and make an impact.
Learn about the Danaher Business System which makes everything possible.
The Senior Technical Writer for Leica Biosystems creates accurate, compliant technical documentation for our Digital Pathology portfolio. Focused on internal and external customer needs, this role develops and maintains user guides, service manuals, and technical instructions that enable the safe, efficient installation, operation, and support of our products. You will collaborate closely with R&D, Quality, Regulatory, and Service & Support stakeholders to translate complex technical data into clear, usable content throughout the product lifecycle. Additionally, this role ensures all materials remain current with strict regulatory and business requirements. This position reports to the Manager, Technical Writing & Training, and is an onsite role based in the Digital Pathology Business Unit in Vista, CA.
This position reports to the Manager, Technical Writing & Training and is part of the Technical Publications Training Team located onsite in the Digital Pathology Business Unit in Vista, CA.
In This Role, You Will Have The Opportunity To
- Own the technical writing swim lane for Digital Pathology programs for NPDs and CRs, acting as the primary writing resource within cross-functional R&D and Service project teams.
- Develop and manage structured single source content using MadCap Flare, covering the full lifecycle from authoring and technical review to localization and release, ensuring high-quality deliverables support the product roadmap.
- Ensure regulatory compliance by creating and maintaining all labeling, including user guides, service guides, and instructions that strictly adhere to FDA, EU MDR/IVDR, and ISO 13485 requirements, ensuring all materials are audit-ready.
- Collaborate with Subject Matter Experts (SMEs) in R&D, Quality, Service and more to translate complex technical specifications into clear, actionable content for both customer-facing and internal service audiences.
- Drive process efficiency by identifying improvements in documentation workflows and styles within the CMS and provide peer review to other writers to ensure consistency and quality across the team.
- Bachelor’s degree in a scientific, technical, or engineering discipline (e.g., Biology, Biomedical Engineering, or Computer Science).
- Prefer minimum of 5 years of experience as a Technical Writer creating documentation for medical devices, diagnostics, or life science instruments.
- Strong working knowledge of medical device regulations and quality standards, including FDA (21 CFR Part 820), EU IVDR/MDR, and ISO 13485.
- Demonstrated expertise with a Content Management System (CMS) or authoring tool, with advanced proficiency in MadCap Flare.
- Excellent verbal and written communication skills with a proven ability to analyze complex topics and translate them into clear, concise, and accurate documentation for diverse audiences.
Ability to travel <10% domestically or internationally
It would be a plus if you also possess previous experience in:
- Working with medical devices or other regulated businesses
- Managing translation outsourcing projects
The annual salary range for this role is $100,000 - $115,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.
#thisisbelonging
#thebestteamisdiverse
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
The U.S. EEO posters are available here.
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.
Salary : $100,000 - $115,000