Bristol myers squibb

Overview

Ensures GMP compliance within Manufacturing by owning documentation, quality events, risk assessments, and inspection readiness activities. The role supports deviation management, change control and audit responses while contributing to defect library training and Communities of Practice.

About Bristol myers squibb

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.

Requirements & Eligibility

• Bachelor’s degree in Life Sciences or related field
• 3-5 years in GMP compliance
• Good collaboration and communication skills
• 3-5 years of experience in pharmaceutical environment
• Business Level in French and English
• Experience in GMP inspections and audits

Key Responsibilities

• Author and maintain manufacturing GMP documentation, including SOPs, forms, and logbooks
• Act as document owner, ensuring lifecycle management and compliance
• Initiate and own activities from initiation to closure for QMS, Change Controls, and findings
• Initiate and own deviations from creation through deviation assessment
• Participate to deviation investigation when needed
• Initiate Supplier Corrective Action Requests (SCARs)
• Participate to Communities of Practice (CoPs)
• Own, perform, and maintain risk assessments, including Manufacturing Risk Assessments and DIRA