Syner-G BioPharma Group is the world's leading provider of chemistry, manufacturing and controls (CMC), regulatory affairs, and medical writing solutions for the biopharma sector. They offer comprehensive services that navigate clients through the complexities of pharmaceutical development, regulatory submissions, and quality compliance, ensuring high-quality outcomes. With a multidisciplinary team, Syner-G integrates science, engineering, and regulatory expertise to support drug development from pre-IND to post-approval phases, enabling timely submissions and patient safety adherence.
cGMP Solutions β’ Regulatory Science for Pharm Development β’ CMC Formulation Development β’ Post-Approval CMC β’ Medical Writing Services
February 5
Join Syner-G as a Senior Regulatory Affairs Specialist focusing on regulatory CMC support through product life cycles.
Remote Jobs at Syner-G BioPharma Group