This position is no longer open for applications

Duties & Responsibilities
• To support the manufacture, optimisation, scale-up and validation of all steps in the monoclonal antibody production process.
• Work with external service providers (CMOs) to provide the necessary technical support for successful completion of projects, including the transfer of the process into the Zoetis facility.
• Support the writing of Batch Manufacturing Records, SOPs, and other quality system documentation required for GMP manufacture.
• Provide hands-on technical support for all manufacturing activities, including buffer/media preparation, cell culture and purification processes.
• Provide technical input and support writing of technical reports required for regulatory purposes.
• Participate in Quality and Safety regulatory audits.
• Identify continuous improvement initiatives and action plans to implement operational excellence and lean practices.