Company Description

TBD Pharmatech, a Contract Development and Manufacturing Organization (CDMO) with 17 years of experience, specializes in the development and production of Active Pharmaceutical Ingredients (APIs), advanced intermediates, and fine chemicals. Operating under EU GMP-compliant standards, TBD combines robust research and development, expertise in validation, and transparent communication, making it a trusted partner for pharmaceutical and biotech companies. The company provides a comprehensive range of services, including route scouting and CMC documentation, with a focus on APIs for generics and Phase 1-2 trial innovative medicines. With a diverse portfolio of over 100 chemical compounds, TBD supports industries in human and veterinary pharmaceuticals and beyond.

Role Description

This is a full-time, on-site Writer role located in Tartu. The Writer will be responsible for creating and editing technical and scientific content, including research publications, technical documentation, marketing materials, and communication for internal and external audiences. The role involves executing content strategies, ensuring accuracy and compliance with regulatory standards, conducting thorough research, and collaborating with cross-disciplinary teams to develop high-quality written materials.

Qualifications

• Strong skills in Technical Writing, Scientific Writing, and Content Editing
• Proficiency in Research, Content Development, and Documentation
• Excellent communication skills, including the ability to simplify technical information for diverse audiences
• Experience with proofreading, reviewing, and ensuring regulatory compliance in written materials
• Background in pharmaceuticals, life sciences, or chemistry is highly beneficial
• Attention to detail and ability to meet deadlines
• Minimum of a Bachelor's degree in Life Sciences, Chemistry, English, Communications, or a relevant field
• Proficiency in English; knowledge of additional languages a plus