Content Writer (Life Sciences & Quality Management)

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.

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.
• Develop content on quality management and regulatory topics relevant to life science companies.
• Translate complex regulatory and quality concepts into clear, accessible content without oversimplifying.
• Proofread and edit your own work and content from other team members to ensure clarity, accuracy, and consistency.
• Collaborate with internal stakeholders to ensure content aligns with SimplerQMS’ positioning, messaging, and quality standards.
• 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).
• 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).
• Proven experience writing professional content in English.

Writing & Language Skills

• Excellent command of written English, with strong attention to grammar, structure, and clarity.
• 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.
• Ability to maintain terminological accuracy while adapting language to different audiences (QA professionals, management, technical teams).
• Strong proofreading and editing skills.

What We Offer

• Fully remote, full-time position (40 hours/week)
• Flexible working hours
• Opportunity to work in a fast-growing, international B2B SaaS company
• Close collaboration with experienced life science and quality professionals
• Structured onboarding and continuous learning
• A supportive, professional, and quality-focused team culture

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.

Meet the Founders

SimplerQMS A/S was founded in 2017 by Allan and Jacob with over 20 years of experience in the Medical Device industry. We have developed SimplerQMS, which enables companies that produce medical devices, health apps, and pharmaceuticals to digitize their documentation processes and spend less time on manual work.