Director, QC Automation
$197.47k - $239.29kBristol Myers Squibb
Bristol Myers Squibb seeks a Director to own the deployment and lifecycle of automated quality control systems across cell therapy manufacturing sites. This role coordinates multi-program priorities, manages vendor relationships, and ensures regulatory compliance while leading cross-functional teams.
Responsibilities
- Own technology roadmap and lifecycle for automated QC equipment and software, including vendor management
- Lead deployment of automated QC systems across cell therapy manufacturing network nodes
- Partner with assay automation and analytical sciences teams to define requirements and resolve issues
- Serve as primary contact for receiving sites, ensuring operational and quality readiness
- Identify deployment risks and drive mitigation plans; ensure cGMP compliance
Requirements
- 12+ years experience in regulated pharmaceutical or biotech manufacturing
- 5+ years leading technology deployment, automation, or tech transfer projects
- In-depth knowledge of cGMP and pharmaceutical regulations
- Experience with automated lab or analytical technologies
- Proven cross-functional team leadership and competing priority coordination
- Strong stakeholder management and influencing skills in matrix organizations
- Solid problem-solving and risk-mitigation capabilities
Compensation: $184,550 - $245,995 base depending on location
$227.13k - $312.9k
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