Job Description
We are looking for a Content Writer who can turn expert input and technical ideas into high-quality articles for our website blog and LinkedIn presence. The focus will be on technical content, case-study style pieces, and platform/product explainer articles tailored to pharma and biotech manufacturing professionals.
This is ideal for someone who enjoys simplifying complex technical or regulatory topics and writing for a B2B SaaS audience.
Key Responsibilities
- Write 24 indepth blog articles per month for our website (1,0001,800 words on average), focused on pharma/biotech quality, validation, and digital systems.
- Create LinkedIn posts and article summaries based on blog content (thought-leadership posts, carousels copy, and short updates).
- Translate complex GxP, validation, and quality management concepts into clear, structured, non-fluffy content for decision-makers and practitioners.
- Repurpose and update existing internal documents, notes, and ideas into polished, publication-ready content (this is not a write from zero with no guidance role).
- Conduct basic research to validate facts, terminology, and current regulatory expectations.
- Apply SEO best practices for blog articles (headlines, subheadings, keywords, meta descriptions) while keeping the writing natural and reader-first.
- Collaborate directly with the Validation Head/founder for briefs, outlines, and feedback and iterate quickly on drafts.
Must-Have Skills and Experience
- Strong command of written English with the ability to write clearly, logically, and persuasively for a professional audience.
- Proven ability to write long-form blog articles and shorter social posts (please share portfolio links or 35 samples).
- Comfortable working from detailed briefs, call notes, and bullet pointsorganising information into a coherent narrative.
- Background or exposure to pharmaceuticals, biotech, medtech, or life sciences, especially in quality, validation, or regulatory affairs
Company Description
Quascenta specializes in providing comprehensive validation lifecycle management software solutions tailored for pharmaceutical manufacturing sites. Our flagship products, eResiduePro, eProcessPro, and eLogBook, revolutionize product, process, and cleaning lifecycle management, ensuring compliance, efficiency, and cost savings. With products designed by industry experts, we not only provide software but also offer expert analysis and recommendations to improve your workflows. Our solutions help simplify residue calculations, track critical processes, and maintain organized validation records. Experience innovative tools designed to meet your unique needs and reach out to learn more.
