About This Role
This position involves working with analytical operations to support clinical and commercial programs, formulation development, quality control testing for GMP operations. As a key member of the team, you will be responsible for various QC activities associated with new product introductions.
Key Responsibilities:
* You will be involved in QC analytical activities, method development & validation, transfer activities, and Process & Cleaning Validation analysis.
* You will provide day-to-day technical support to operations for deviations, investigations, optimisation programs etc
Requirements
* Relevant experience in test methods for biologic and biopharmaceutical products
* Strong knowledge and understanding of cGMP, quality control (QC), and regulatory requirements for GMP laboratories
* Advanced knowledge of current Good Laboratory Practices (GLPs) and current Good Manufacturing Practices (GMPs)