Pharmaceutical Development Scientist

Company Description

Bio Health Group is a Wyoming, USA-based pharmaceutical and biologics development company dedicated to advancing regulated programs. The organization emphasizes practical technical execution, quality-focused documentation, rigorous analytical oversight, and robust process development support. Work at Bio Health Group centers on structured research planning, supplier qualification, technical review, and scale-up readiness for regulated products. By combining deep scientific expertise with strong regulatory discipline, the team delivers consistent, compliant, and development-ready outcomes that support successful clinical and commercial advancement.

This is a full‑time, on‑site Pharmaceutical Development Scientist role based in Cheyenne, WY. The individual in this role will design and execute laboratory studies to support pharmaceutical and biologics development, including method development, formulation studies, process characterization, and stability assessments. Day‑to‑day responsibilities include planning and conducting experiments, documenting work to GMP and regulatory standards, analyzing data, and preparing technical reports, protocols, and summaries for internal and external stakeholders.

The role involves supporting technology transfer and scale‑up activities, collaborating with cross‑functional teams (e.g., quality, manufacturing, regulatory), and contributing to risk assessments and technical reviews for regulated programs. The scientist will also help optimize processes, troubleshoot technical issues, and maintain a safe, compliant, and well‑organized laboratory environment.

• Strong Laboratory Skills and hands‑on experience with pharmaceutical and/or biologics development techniques.
• Demonstrated background in Research and Development (R&D) and research, including experimental design, execution, and documentation.
• Working knowledge of Good Manufacturing Practice (GMP) principles and experience operating in or supporting regulated environments.
• Proficiency in Data Analysis, including statistical interpretation of experimental results and use of common scientific software tools.
• Bachelor’s, Master’s, or PhD in Pharmaceutical Sciences, Chemistry, Biochemistry, Chemical Engineering, or a related scientific discipline.
• Ability to write clear technical reports, protocols, and standard operating procedures with strong attention to detail and data integrity.
• Effective collaboration and communication skills, with the ability to work in cross‑functional teams and manage multiple priorities.
• Experience with process development, scale‑up, or tech transfer for small molecules or biologics is preferred.
• Familiarity with regulatory expectations for regulated pharmaceutical or biologics programs (e.g., clinical development, CMC documentation) is an advantage.