Become a Specialist in Deviation Management at Resilience, focusing on investigating and authoring deviation reports within a biomanufacturing context.
In this critical role, you will take charge of identifying and resolving quality deviations, supporting continuous operational improvements in pharmaceutical production. Your experience in Root Cause Analysis and regulatory compliance will be essential for maintaining high manufacturing standards. Effective collaboration with internal teams and clients will be key to ensuring timely resolution of quality issues.
Key Responsibilities:
• Manage and investigate deviations and document findings
• Develop strategies for Root Cause Analysis using data
• Ensure timely closure of deviation reports and investigations
• Liaise with stakeholders to support quality processes
• Verify compliance with cGMP regulations in manufacturing
Requirements:
• Diploma with 3+ years or a B.Sc. in a related field
• Proven track reco...