We are looking for a CMC officer to join our Product Development team in Athens, Greece. This is a full-time, on-site position where you will play a key role in coordinating, compiling, and reviewing important regulatory documents (CTD) for pharmaceutical products. If you’re passionate about working in a dynamic, collaborative environment, this could be the perfect role for you!
Your main responsibilities will include:
- Coordinating, compiling, and reviewing CTD for pharmaceutical products
- Supporting dossier submissions and working closely with lab and production teams
- Ensuring all processes follow regulatory guidelines and deadlines
What we’re looking for:
- Bachelor’s degree in Sciences (Pharmacy or Chemistry preferred)
- 2+ years of experience in dossier compilation within the pharmaceutical industry
- Fluency in English (written and oral)
- Strong computer skills (MS Office)
- Excellent organizational and multitasking skills
- Ability to work under deadlines and as part of a team
Send us your CV to hr@kleva.gr