Opportunity Description
Be a key player in biomanufacturing at OmniaBio as an Associate I in Commissioning, Qualification, and Validation. Elevate your career by ensuring compliance with GMP and supporting innovative therapy development.
This role demands expertise in validating master plans and developing qualification documentation alongside interdisciplinary teams. Your contributions will enhance our cell-based therapies and support a fast-paced environment, while ensuring that all regulatory requirements are met in documentation and procedures.
Key Responsibilities:
• Develop validation master plans and deliverables
• Engage with stakeholders to create compliant documentation
• Schedule and maintain validation activity timelines
• Draft SOPs and manage preventive maintenance programs
• Conduct internal audits and support risk assessments
Requirements:
• Minimum 1 year of experience in a related CQV role
• Preferred education ...
This role demands expertise in validating master plans and developing qualification documentation alongside interdisciplinary teams. Your contributions will enhance our cell-based therapies and support a fast-paced environment, while ensuring that all regulatory requirements are met in documentation and procedures.
Key Responsibilities:
• Develop validation master plans and deliverables
• Engage with stakeholders to create compliant documentation
• Schedule and maintain validation activity timelines
• Draft SOPs and manage preventive maintenance programs
• Conduct internal audits and support risk assessments
Requirements:
• Minimum 1 year of experience in a related CQV role
• Preferred education ...
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