Medical Writer India, Mexico, Brazil

Job Title: Medical Writer - Fixed Term Contract (12 months, Full Time) Locations: India, Mexico, Brazil Department: Scientific Operations About the Role: We are seeking a Medical Writer to join a dynamic scientific operations team supporting medical device projects. This is a full-time, site-based role on a 12-month fixed-term contract with the potential for extension. The Medical Writer will create, update, and manage a range of regulatory and clinical documents including Clinical Evaluation Reports (CERs), Summary of Safety and Clinical Performance Reports (SSCPs), State of the Art Reviews (SOAs), and Systematic Literature Reviews (LRRs) within their assigned therapeutic area. Key Responsibilities: • Write and update CERs, SSCPs, SOAs, and LRRs in compliance with applicable regulatory requirements and guidelines • Participate in all core steps of systematic literature reviews, including search, screening, data extraction, analysis, and synthesis • Summarize clinical, non-clinical, and regulatory data to perform risk/benefit analyses on medical devices • Compare device safety and performance against the state of the art and investigate unexpected outcomes • Utilize various software systems, including Microsoft Office, EndNote, Distiller, Wrike, and in-house AI tools, to create required documents • Follow all company procedures, regulatory guidelines, and health, safety, and environmental practices • Collaborate with cross-functional teams including Medical Directors, Post Market Surveillance, Design Quality Engineers, R&D, and Regulatory Affairs • Communicate business-related issues or opportunities to management effectively Education & Experience Requirements: • BA, BS, or BSN required; advanced degree preferred • Minimum of 3 years’ experience in medical writing or related roles • Experience in the medical device industry and knowledge of CER regulatory requirements, evidence generation, and literature reviews preferred • Familiarity with clinical research, quality/regulatory compliance, and adverse event reporting is a plus • Strong oral communication, presentation, project management, and prioritization skills Additional Qualifications/Desirable: • Background in life sciences (Dentistry, Optometry, Veterinary Science, etc.) is welcomed • Experience with CER creation, MEDDEV 2.7.1 rev 4, MDCG/MDR regulations considered a strong advantage • Proven ability to perform literature searches, summarize clinical conditions, and assess risks and benefits for medical devices • Experience reviewing supporting device documentation and analyzing device performance data This is an exciting opportunity for a detail-oriented professional to contribute to regulatory and scientific documentation within the medical device sector while working in a collaborative, cross-functional environment. Must-Haves: * Minimum of 3 years’ experience in medical writing or regulatory documentation, preferably in medical devices. * Experience writing Clinical Evaluation Reports (CERs), Summary of Safety and Clinical Performance Reports (SSCPs), State of the Art Reviews (SOAs), or Systematic Literature Reviews (LRRs). * Strong understanding of clinical data, non-clinical data, and regulatory requirements for medical devices. * Proficiency in Microsoft Office and literature review tools (EndNote, Distiller, Wrike, or similar). * Strong communication, presentation, project management, and prioritization skills. Nice-to-Haves: * Experience with MEDDEV 2.7.1 rev 4, MDCG/MDR, or other medical device regulatory frameworks. * Background in life sciences (Dentistry, Optometry, Veterinary Science, or similar). * Experience performing systematic literature searches and data extraction across multiple therapeutic areas. * Knowledge of adverse event reporting and risk/benefit analysis for medical devices. * Familiarity with cross-functional collaboration with Medical Directors, Post Market Surveillance, R&D, and Regulatory Affairs teams.