Medical & Technical Content Writer
Medical & Technical Content Writer
22
Hyderabad, Telangana, India
Job Views:
Created Date: 2026-10-12
End Date:
Experience: 3 - 5 years
Salary: 500000
Industry: Others
Openings: 1
Primary Responsibilities :
Data translation: Synthesize extraction parameters, phytochemical characterization, analytical methods,
bioassays, and preclinical findings into clear scientific narratives.
Technical dossiers: Author and maintain product monographs, technical data sheets, white papers, MoA
summaries, FAQs, slide decks, and study summaries.
Evidence management: Conduct structured literature reviews, assess study quality and relevance,
manage references, and maintain evidence-to-claim traceability.
Claims support: Draft scientifically defensible structure-function wording within US dietary supplement
boundaries, in partnership with Regulatory.
Study documentation: Support protocol synopses, investigator briefs, reports, abstracts, posters, and
publication-ready summaries for in-vitro and in-vivo work.
Customer support: Draft responses for technical questionnaires and scientific queries from customer
R&D, QA, and Regulatory teams.
Cross-functional control: Maintain approved language, document versions, review workflows, source
files, and consistency across scientific and commercial materials.
Experience Requirements:
Education: Master’s degree or PhD in Pharmacology, Biochemistry, Biotechnology, Life Sciences,
Pharmacy, or a closely related discipline.
Experience: 3-5 years in medical writing, scientific communications, regulatory writing, or technical
documentation in nutraceuticals, phytomedicine, botanical drugs, or pharma.
Scientific reasoning: Able to interpret assay design, controls, endpoints, dose-response data, statistical
outputs, limitations, and biological relevance.
Writing quality: Excellent English, precise citation practice, strong document architecture, and ability to
adapt one evidence base for scientific and commercial audiences.
Regulatory awareness: Practical understanding of structure-function claims, substantiation, DSHEA
boundaries, and the distinction between ingredient evidence and finished-product claims.
Tools: Proficiency with reference managers and document collaboration/version-control workflows.
Non-Negotiable Hiring Criteria
Submitted writing samples showing technical or medical authorship; generic blogs alone are insufficient.
Ability to critically interpret primary research and preclinical data rather than merely summarize abstracts.
Experience working with scientific, quality, regulatory, or clinical stakeholders through review cycles.
No plagiarism, invented citations, overstatement, or disease-treatment language.
Preferred / Advantageous
Experience with botanical standardization, phytochemistry, natural products, or dietary supplement
ingredients.
Publication, poster, protocol, or technical dossier experience.
Familiarity with PubMed, Zotero/EndNote/Mendeley, and AI-assisted research with rigorous human
verification.
Understanding of common analytical techniques such as HPLC/UPLC, LC-MS, spectroscopy, or validated
bioassays.
