✨ The Role in One Sentence

We are seeking a CMC Technology Transfer Specialist to lead the implementation of drug product manufacturing processes at clinical trial locations.

📋 What You'll Likely Do

• 30%: Prepare and maintain documentation, including technology transfer packages and validation plans.

• 30%: Oversee clinical site set-up and validation activities, ensuring regulatory compliance.

• 20%: Coordinate interactions with third-party CDMOs to support outsourced activities.

🧑‍💻 Profiles Doing This Job

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

• High Priority: 5+ years' experience in pharmaceutical manufacturing or technology transfer.

• High Priority: Strong understanding of GMP and ICH guidelines.

📈 How This Role Will Look on Your CV

• Led technology transfers and supported GMP manufacturing at clinical scale.