Biologic Manufacturing Engineer Specialist, Morrisville

Drive advancements in gene therapy as a Manufacturing Engineer. Oversee vital production processes, maintain compliance, and elevate operational standards within cGMP environments.

This critical role entails managing batch production from inception to completion, ensuring high-quality outputs that adhere to regulatory standards. You will be responsible for troubleshooting and authoring vital documentation, along with supporting tech transfers and training initiatives. Your engineering insight will help streamline processes and enhance operational efficiency.

Key Responsibilities:• Execute comprehensive batch production and operations • Maintain compliance through effective documentation practices • Troubleshoot production issues and escalate as needed • Author and oversee Standard Operating Procedures (SOPs) • Collaborate with supply chain for operational readiness

Requirements:• At least 2 years in a cGMP setting • Strong team collaboration and communication skills • Ability to adapt to changing priorities • Physical capacity to lift up to 50 pounds • Bachelor’s degree in Engineering or Life Sciences encouraged

Contribute your manufacturing expertise and be part of a team that is transforming patient care through innovative gene therapies. #J-18808-Ljbffr