Transform biomanufacturing with OmniaBio as an Associate I, focusing on Commissioning, Qualification, and Validation activities. Engage in essential documentation compliance and contribute to our innovative cell and gene therapies.
In this role, you will support the development of validation master plans and ensure all deliverables adhere to Good Manufacturing Practices (GMP). Collaborating with key stakeholders, from Manufacturing Science to Quality Assurance, you will help develop documentation and schedules for validation activities while managing changes and assessments effectively.
Key Responsibilities:
• Validate master plans for equipment and processes
• Collaborate with internal teams on documentation
• Maintain validation activities schedules
• Develop standard operating procedures (SOPs)
• Participate in internal audits as a subject matter expert
Requirements:
• 1+ years in a biopharma GMP environment
• Post-secondary education in engineering tec...