Director, QC Automation
Bristol Myers Squibb · Devens, MA +3 more
QualityFull-time$197k–$239kCompany career page
The apply link worked recently (not employer-confirmed).
What they're looking for
- 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
What you'll be doing
- 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
Privacy & handoff
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