✨ The Role in One Sentence

Join us as a CMC Process Development Specialist to develop and validate manufacturing processes and reagent kits, ensuring compliance and scalability.

📋 What You'll Likely Do

• 30%: Manage scale-up and optimization of manufacturing workflows to meet regulatory requirements.

• 30%: Oversee CDMO partnerships, ensuring efficient development and technology transfer.

• 40%: Prepare and review CMC-related documents, ensuring compliance with GMP, GLP, and ICH guidelines.

🧑‍💻 Profiles Doing This Job

• High Priority: MSc or PhD in pharmaceutical sciences, chemical engineering, or related field.

• High Priority: 3+ years in process development, manufacturing, or related role in pharma/biotech.

• High Priority: Expertise in CMC development, tech transfer, and manufacturing process validation.

📈 How This Role Will Look on Your CV

• Managed CMC process development, ensuring regulatory compliance and successful technology transfer.