Associate Technical Writer

Posted 12 Days Ago
Be an Early Applicant
Taguig City, Fourth District NCR, National Capital Region, PHL
In-Office
Junior
Biotech
The Role
Creates, edits, formats, validates, and maintains technical documentation including manuals, instructions, product literature, quick-reference guides, and online help. Collaborates with subject-matter experts and cross-functional teams, coordinates quality-system reviews and approvals, tracks documentation deliverables, and manages version control, publishing, templates, and archiving. The role also improves content accuracy, usability, consistency, and compliance, with opportunities to lead complex documentation projects.
Summary Generated by Built In

Overview  

 
At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible.  

We’re dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We’re always striving to identify talented individuals to join our exceptional teams. 
 
We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you. 

 

At QIAGEN, every day is an opportunity to make a real-life impact. 

 

Join us, grow with us, and together, let's shape the future of biological discovery. 

‎

About the opportunity

Join our Content Marketing team and help create clear, accurate, and user-friendly technical documentation that supports QIAGEN products and customers. In this temporary position, you will work closely with Research and Development, Product Management, Design, Quality, and Marketing stakeholders to develop and maintain product literature. The contract is expected to run for six to twelve months, with work performed on an EU or mid-shift schedule. Two positions are available.

Your tasks include

  • You create, edit, format, and maintain technical documentation, including user manuals, instructions for use, quick-reference guides, product literature, and online help materials.
  • You gather, analyze, and validate technical information in close collaboration with subject-matter experts and cross-functional stakeholders.
  • You plan, schedule, and track documentation activities to support product release dates and agreed deliverables.
  • You coordinate document review and approval activities through the Quality Management System.
  • You review existing documentation to improve its accuracy, usability, consistency, readability, and alignment with applicable quality requirements.
  • You support document lifecycle activities, including version control, publishing, template maintenance, and archival processes.
  • Depending on your experience, you lead complex documentation projects, manage stakeholder expectations, improve content standards, and provide guidance to less-experienced writers.

Your profile

  • You hold a bachelor’s degree in Technical Communication, English, Journalism, Life Sciences, Computer Science, Marketing, or a related discipline.
  • You bring at least two years of experience in technical writing, copy editing, content development, documentation management, or a comparable role. For the Technical Writer level, five or more years of relevant experience is preferred.
  • You can translate complex technical information into clear, concise, accurate, and accessible documentation.
  • You have strong Microsoft Word formatting skills and experience using documentation tools, content management systems, or collaborative authoring platforms.
  • You can coordinate documentation projects, manage priorities, and communicate effectively with stakeholders to deliver high-quality work on schedule.
  • Experience in a regulated, scientific, healthcare, software, or technology environment is an advantage.
  • Experience with MadCap Flare, Adobe Creative Cloud, particularly Photoshop and InDesign, or comparable authoring tools is a plus.

What we offer  

 

  • Bonus/Commission  

  • Local benefits   

  • Referral Program  

  • Volunteer Day  

  • Internal Academy (QIALearn)   

  • Employee Assistance Program   

  • Hybrid work (conditional to your role) 

 

Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve. We inspire with our leadership and make an impact with our actions. We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking.   

 

QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.  

Skills Required

  • Bachelor's degree in Technical Communication, English, Journalism, Life Sciences, Computer Science, Marketing, or a related discipline
  • At least two years of experience in technical writing, copy editing, content development, documentation management, or a comparable role
  • Ability to translate complex technical information into clear, concise, accurate, and accessible documentation
  • Strong Microsoft Word formatting skills
  • Experience using documentation tools, content management systems, or collaborative authoring platforms
  • Ability to coordinate documentation projects, manage priorities, and communicate effectively with stakeholders
  • Five or more years of relevant experience for the Technical Writer level
  • Experience in a regulated, scientific, healthcare, software, or technology environment
  • Experience with MadCap Flare, Adobe Creative Cloud, Photoshop, InDesign, or comparable authoring tools

QIAGEN Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about QIAGEN and has not been reviewed or approved by QIAGEN.

  • Flexible Benefits — Flexible work options (hybrid or remote where roles allow), flexible hours, sabbaticals, and site-specific childcare support work–life fit. Programs are presented as available where roles allow, signaling adaptable benefit design.
  • Wellbeing & Lifestyle Benefits — A global Employee Assistance Program for employees and immediate family, alongside broader wellbeing initiatives and community volunteering time, provides everyday support. Recognition for inclusive culture reinforces the emphasis on a supportive environment.
  • Parental & Family Support — Paid parental leave positioned as above typical U.S. norms and family-oriented offerings (e.g., on-site childcare at some locations) enhance caregiver support. Reports of solid PTO and holidays further strengthen family time.

QIAGEN Insights

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The Company
HQ: Hilden
6,000 Employees
Year Founded: 1984

What We Do

QIAGEN is the leading global provider of Sample to Insight solutions that enable customers to gain valuable molecular insights from samples containing the building blocks of life. Our sample technologies isolate and process DNA, RNA and proteins from blood, tissue and other materials. Assay technologies make these biomolecules visible and ready for analysis. Bioinformatics software and knowledge bases interpret data to report relevant, actionable insights. Automation solutions tie these together in seamless and cost-effective workflows. QIAGEN provides solutions to more than 500,000 customers around the world in Molecular Diagnostics (human healthcare) and Life Sciences (academia, pharma R&D and industrial applications, primarily forensics).

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