At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a highly motivated and detail-oriented R&D CMC Officer to join our team.

Main duties and responsibilities:

• Prepare CMC technical documents in accordance with FDA requirements
• Collect and evaluate scientific data
• Conduct extensive literature research and studying of scientific documents
• Act as a liaison with Regulatory Teams
• Understand Regulatory strategy and documentation requirements

Experience, skills and qualifications required:

• BSc Degree in Chemistry, Biology or relevant field.
• 1+ years of experience in CMC within a Pharmaceutical organization.
• Scientific/technical writing skills
• Fluent in English and good MS Office skills
• Strong organization skills, multi-tasking and able to meet deadlines
• Effective communication and relationship management
• Knowledge of GMP and CMC guidelines
• Ability to work under pressure, resilience

The Company offers competitive remuneration, continuous learning and development opportunities, and a friendly and challenging working environment. All applications will be considered as strictly confidential