THIS IS WHERE YOU SAVE AND SUSTAIN LIVES

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.
Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.
Your role at Baxter
This position is responsible for ensuring that CIVA is compliant with NAPRA, cGMP, applicable license(s) and the Baxter Quality Management System. As the Sterile Compounding Supervisor, this position develops, organizes and oversees all activities related to sterile-preparation compounding. This role will be primarily focused on Quality Operations, while supporting Quality Systems.

What you will be doing

• Collaborate with Operations to assess quality risk and address compliance gaps.
• Lead resolution of daily operational quality issues and provide product disposition in a timely manner.
• Apply expertise in critical production areas to ensure timely and efficient product release.
• Maintain audit-ready state and host/participate in internal and external audits.
• Provide Quality support to CIVA projects
• Perform other Quality duties as assigned

Sterile Compounding Supervisor

• Perform all functions of Sterile Compounding Supervisor per NAPRA Model Standards for Pharmacy Compounding of Hazardous/Non-Hazardous Sterile Preparations
• Main point of contact for all communications with OCP
• Lead execution of and response to annual OCP inspection
• Assess proposed changes for compliance to NAPRA requirements
• Review and approve semi-annual cleanroom/PEC certifications, daily/weekly/monthly cleaning logs, semi-annual process simulations, monthly EM trend report

Complaints

• Log and track external and B2B complaints
• Liase with Product Surveillance to effectively process complaints
• Manage the return of complaint samples
• Complete evaluation of complaint samples, perform manufacturing record review and investigations, as necessary
• Update metrics

• Collaborate with Operations to assess quality risk and address compliance gaps.
• Lead resolution of daily operational quality issues and provide product disposition in a timely manner.
• Apply expertise in critical production areas to ensure timely and efficient product release.
• Maintain audit-ready state and host/participate in internal and external audits.
• Provide Quality support to CIVA projects
• Perform other Quality duties as assigne