Content Writer – Life Sciences & Quality Management

About SimplerQMS

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 that 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

How to Apply

To apply, please:

1. Click Apply
2. Submit your CV

Qualified candidates will go through a structured selection process, which may include a short writing assignment and interviews.

Thank you for considering a career at SimplerQMS.

We look forward to learning how your writing and life science experience can contribute to our team.