Join Aspect Biosystems as a GMP Quality Assurance Specialist and oversee quality for cutting-edge bioprinted therapies. Your expertise will ensure compliance and improvement in manufacturing practices.
We are searching for a Quality Assurance Specialist to support our quality management system and develop robust internal QA processes. The role requires collaboration with R&D; and cross-functional teams, providing insight and expertise on quality assurance during product design and development. Solid attention to detail and experience with GMP in the biotech industry are essential for success.
Key Responsibilities:
• Support implementation of the Quality Management System • Provide document control and maintain compliance • Develop training for QA processes and certifications • Conduct risk assessments on core raw materials • Review and approve incoming raw materials specifications
Requirements: • Bachelor’s or Master’s degree in relevant discipline • Minimum 5-7 years of GMP experience • Understanding of FDA and regulatory authorities • Strong attention to detail and process control • Proactive team collaboration and communication
Your expertise will be vital in advocating quality assurance within our innovative bioprinted therapies at Aspect. #J-18808-Ljbffr