Open Position:
Full-Time (Remote)
SimplerQMS is a Denmark-based SaaS company providing an Electronic Quality Management System (eQMS) purpose-built for life science companies. We help organizations in pharmaceuticals, biotechnology, and medical devices work more efficiently while supporting compliance with regulatory requirements.
Our mission is simple: make quality management easier, so life science companies can focus on innovation and growth.
As we continue to expand globally, we are looking for a skilled Content Writer with hands-on life science quality management experience to strengthen our marketing content and help us communicate complex topics clearly and accurately.
About the Role
We are looking for a content professional who combines excellent English writing skills with practical exposure to Quality Assurance (QA) and/or Regulatory Affairs (RA) in regulated life science environments.
In this role, you will create high-quality, accurate, and educational content that helps our audience understand quality management concepts and how SimplerQMS supports their daily work. While this is not a QA or RA operational role, your domain knowledge will be essential for producing credible, trustworthy content.Â
You will be part of the Marketing team and work closely with subject-matter experts, product marketing, and commercial teams.
What You’ll Do
- Write high-quality, well-structured English content, with blog articles as your primary focus.Â
- Develop content on quality management and regulatory topics relevant to life science companies.Â
- Translate complex regulatory and quality concepts into clear, accessible content without oversimplifying.Â
- Proofread and edit your own work and content from other team members to ensure clarity, accuracy, and consistency.Â
- Collaborate with internal stakeholders to ensure content aligns with SimplerQMS’ positioning, messaging, and quality standards.Â
- Continuously improve content quality based on feedback, performance insights, and evolving best practices.
Qualifications
Required Experience
- Hands-on experience working with Quality Assurance (QA) and/or Regulatory Affairs (RA) activities in life science industries (pharmaceuticals, biotechnology, medical devices, or related regulated environments).Â
- Practical understanding of how a QMS is used in regulated operations (e.g. working with SOPs, audits, CAPAs, deviations, change control, training records, or supplier documentation).Â
- Proven experience writing professional content in English.Â
Writing & Language Skills
- Excellent command of written English, with strong attention to grammar, structure, and clarity.Â
- Solid understanding of lexical relationships (e.g. synonyms, antonyms, hyponyms, related terminology) and the ability to use them deliberately to create precise, varied, and consistent content.Â
- Ability to maintain terminological accuracy while adapting language to different audiences (QA professionals, management, technical teams).Â
- Strong proofreading and editing skills.Â
What We Offer
- Fully remote, full-time position (40 hours/week)Â
- Flexible working hoursÂ
- Opportunity to work in a fast-growing, international B2B SaaS companyÂ
- Close collaboration with experienced life science and quality professionalsÂ
- Structured onboarding and continuous learningÂ
- A supportive, professional, and quality-focused team cultureÂ
If this is your dream, then we’d love to hear from you.
Please send an email to gf@simplerqms.com with your resume or reach out to Germans Frolovs at +4552810035 if you have any questions.