Shape healthcare standards at Baxter as the Lead Sterility Assurance Specialist. Ensure compliance and lead initiatives that impact lives across the globe in a GMP regulated workplace.
In this pivotal role, you will oversee CIVA's Sterility Assurance program, ensuring alignment with Baxter Corporate standards and regulatory requirements. With 3-5 years of experience in a GMP setting, you will investigate sterility assurance exceptions and direct the Environmental Monitoring program. This role requires strong leadership and mentorship capabilities, alongside analytical and problem-solving skills.
Key Responsibilities:
• Ensure compliance with sterility assurance and regulatory requirements
• Direct and maintain the Environmental Monitoring program
• Represent sterility assurance at forums and practice communities




• Investigate all sterility assurance-related exceptions
• Lead cross-functional performance qualifications and risk assessments
Requirements:
• Bachelor of Science in Pharmacy, Microbiology, Chemistry, or Biology
• 3-5 years of relevant GMP industry experience
• Strong understanding of aseptic techniques and GMP
• Excellent problem-solving and analytical abilities
• Experience in cleanrooms and aseptic processing preferred
Join Baxter to drive quality and compliance in healthcare delivery through your expertise in sterility assurance.
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📌 Lead Sterility Assurance Specialist at Baxter (Mississauga)
🏢 Baxter International
📍 Mississauga