Associate Scientific Writer – CMC Drug Product

Role Overview

• Write and compile scientific and technical documents related to drug product development such as Writing the documents.
• Data analysis.
• Coordination of the review and approval activities.
• Making sure timelines are met.
• Ensuring that the documentation is of high quality and that potential issues are discussed with the customers.

Requirements

• Master’s degree in Pharmaceutical Sciences.
• Passion for scientific and technical writing for chemical and biopharmaceutical products.
• Strong interest in drug development and regulatory guidelines.
• Very good communication skills (both written and spoken).
• Fluent in written and spoken English.
• Strong scientific writing skills.
• Attention to detail and accuracy.
• Eager to learn and ability to work independently when necessary.
• Proficient in MS Office (primarily Word and Excel).
• Problem-solving skills with a quality-conscious attitude.
• Well-organized with the ability to work in a dynamic environment.

Benefits

• Opportunity to contribute to the development of new drugs.
• A supportive learning environment for skill development and growth.
• Involvement in a rapidly growing international company with an intriguing services, product, and customer portfolio.
• Dynamic working environment with friendly and collaborative colleagues.
• Open, straightforward, and caring company culture.
• Attractive remuneration package.
• Flexible working hours and the possibility for partial telework.
• Generous annual leave entitlement of 32 days.