This role supports cGMP Manufacturing Operations for the BMS Bothell site, focusing on coordination, issuance, reconciliation, and management of production labels and records
Job Summary
This role supports cGMP Manufacturing Operations for the BMS Bothell site, focusing on coordination, issuance, reconciliation, and management of production labels and records.
Key responsibilities include developing, performing, and maintaining a GMP compliant clinical and commercial batch documentation and label issuance and control process.
Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs that provide employees with the resources to pursue their goals, both at work and in their personal lives.
Matching Summary
This role supports cGMP Manufacturing Operations for the BMS Bothell site, focusing on coordination, issuance, reconciliation, and management of production labels and records.
Salary
Base: $96,832 - $117,338; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits
Skills & Requirements
Must-have
cGMP compliant batch documentation
production label issuance
batch record control
quality systems management
document change requests
Nice-to-have
innovative and proactive approach
continuous improvement mindset
collaborate with cross-functional departments
role model culture of compliance
Key Requirements
3+ years cGMP/FDA regulated environment experience