Position Overview We are seeking a motivated
Scientific Writer / Medical Affairs Specialist
to join our team. The role requires experience in medical writing, regulatory documentation, and the ability to translate complex scientific information into clear, accurate, and compliant materials for internal stakeholders and external audiences.
Key Responsibilities Develop, review, and publish scientific and medical content in line with company and regulatory standards. Manage documentation within
Veeva Promomats
and ensure compliance with
MLR (Medical, Legal, Regulatory) review processes
. Analyze and verify that information published on websites is accurate, up to date, and consistent with client requests. Review promotional and non-promotional materials to ensure alignment with scientific evidence and regulatory requirements. Conduct literature reviews, interpret scientific articles,



and prepare standard response documents (SRDs). Collaborate effectively with cross-functional teams (Medical Affairs, Regulatory, Marketing).
Qualifications ~ Experience: ~2–3 years in the pharmaceutical industry (Medical Services, Medico-Marketing, Clinical Research, Regulatory Affairs, or Medical Writing) ~
OR ~2–3 years in clinical practice ~ Hands-on experience with
Veeva Promomats
and
MLR documentation processes
. ~ Strong ability to analyze scientific content and ensure accuracy across multiple platforms. ~ Preferred: Academic publications or conference presentations. ~ Bilingual proficiency: English (required), Portuguese or other languages a plus.

📌 Grant writer - scientific writer (Ciudad de México)
🏢 Greymatter Innovationz
📍 Ciudad de México