Trilogy Writing & Consulting is currently looking to hire an experienced Quality Control Specialist to perform quality control of nonclinical and clinical regulatory documents. The position (onsite or remote) would support our growing company in producing regulatory documentation for the international pharmaceutical industry.

Applicants must live in one of the following countries: Germany, UK, USA, Canada, Portugal, Italy, Ireland, and must have the following skills and experience:

Responsibilities for this position will include:

Trilogy Writing is a dynamic, growing company focused on medical writing of regulatory documents. We provide services to a solid, international customer base that includes a broad range of pharmaceutical companies that are among the best-known names in the European and US pharmaceutical industry. We value our people and offer a competitive salary and a wide range of benefits. 

To apply, please write in English, specifying how you comply with the experience requirements, with your CV at 

Trilogy Writing & Consulting is an equal opportunity employer. Our company values are based on inclusivity and diversity, and we do not discriminate or allow discrimination on the basis of race, color, religion, sex, age, sexual orientation, gender identity, national origin, citizenship, marital status, disability, or any other characteristic protected by law. We passionately believe in creating a supportive environment in which everyone can grow, flourish, and do their best work.