Found Description
Join OmniaBio as an Associate I, specializing in Commissioning, Qualification, and Validation. Contribute to our mission of transforming biomanufacturing through your expertise in compliance and documentation.
In this role, your responsibilities will include developing validation master plans and ensuring all equipment and processes comply with GMP standards. Working collaboratively with key departments, you will create and manage necessary documentation while also preparing for audits and assessments required for our innovative therapies.
Key Responsibilities:
• Validate development of equipment and system qualifications
• Collaborate to establish documentation requirements
• Keep track of validation schedules and deadlines
• Prepare temperature mapping protocols
• Support completion of change controls and assessments
Requirements:
• At least 1 year in a biopharma GMP setting
• Post-secondary education in...
In this role, your responsibilities will include developing validation master plans and ensuring all equipment and processes comply with GMP standards. Working collaboratively with key departments, you will create and manage necessary documentation while also preparing for audits and assessments required for our innovative therapies.
Key Responsibilities:
• Validate development of equipment and system qualifications
• Collaborate to establish documentation requirements
• Keep track of validation schedules and deadlines
• Prepare temperature mapping protocols
• Support completion of change controls and assessments
Requirements:
• At least 1 year in a biopharma GMP setting
• Post-secondary education in...