Regulatory Affairs Specialist

Excelya is hiring a Regulatory Affairs Specialist to support regulatory submissions, ensure compliance with international regulations, and assist in clinical or pharmaceutical projects. The role involves documentation management, coordination with teams, and maintaining regulatory standards.

Prepare and manage regulatory documentation, support submissions, ensure compliance with regulations, coordinate with internal teams, and assist in clinical or pharmaceutical processes.

Experience in regulatory affairs, knowledge of clinical or pharmaceutical regulations, strong documentation skills, attention to detail, and ability to manage deadlines.

Excelya is a global consulting and services company specializing in life sciences, providing support across clinical research, regulatory affairs, quality management, and market access. The company partners with pharmaceutical, biotechnology, and medical device organizations to accelerate product development and ensure compliance with industry standards. Excelya combines scientific expertise with tailored consulting solutions to support the full lifecycle of healthcare innovation.