Associate Scientific Writer: Turn Data into Clear Science

caprion; Antwerpen; On-site; EUR 42,000 - 60,000; Full time

Job summary

CellCarta is seeking an Associate Scientific Writer in Antwerpen to help craft high-quality scientific and technical documents, including study and validation reports, posters, and data presentations. You will translate complex concepts into accessible content and learn regulatory requirements across ISO 13485, ISO 15189, CAP/CLIA, GxP, 21 CFR Part 820, and IVDR.

You will work with the Scientific Writing team to draft, review, and finalize documents, participate in literature reviews, and

Qualifications

• Master’s degree in a scientific field with strong interest in scientific writing or a Bachelor’s in a scientific field with prior technical writing experience
• Demonstrates ability to learn and grasp technical concepts
• Proficient in Microsoft Office and documentation tools
• Strong verbal and written communication skills and meticulous attention to detail

Responsibilities

• Assist with writing scientific and technical documentation including validation reports, study reports, posters, data presentations, and training materials
• Ensure documents meet ISO 13485, ISO 15189, CAP/CLIA, GxP, 21 CFR Part 820, IVDR requirements
• Collaborate with SMEs and QA reviewers; implement feedback per quality guidelines
• Prepare factual literature summaries and convert data into clear narratives with tables, graphs, and images
• Create PowerPoint presentations summarizing study details and conclusions

Skills

Microsoft Office

Technical writing

Communication skills

Attention to detail

Organizational skills

Independent worker

Multitasking

Education

Master’s or Bachelor's in science

Job description

CellCarta is seeking an Associate Scientific Writer in Antwerpen to help craft high-quality scientific and technical documents, including study and validation reports, posters, and data presentations. You will translate complex concepts into accessible content and learn regulatory requirements across ISO 13485, ISO 15189, CAP/CLIA, GxP, 21 CFR Part 820, and IVDR.

You will work with the Scientific Writing team to draft, review, and finalize documents, participate in literature reviews, and