Supervisor-I, MFG Day Shift (Monday to Friday 07:00 - 15:00)

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.

We need a full-time Supervisor-I, MFG, Day Shift (Monday to Friday 07:00 - 15:00). You will lead a dynamic team in a fast-paced manufacturing environment. You'll work with automated equipment and ensure quality and efficiency.

Key Responsibilities

The Filling Supervisor coordinates the filling of high-volume IV codes using highly sophisticated automated equipment. They apply their expertise to monitor the activities of team members and machinery to fill the required amount of product at the least cost, consistent with quality standards and specifications. The position is responsible for the cleaning and sanitization of the equipment and facility in this area. They use Baxter’s Shared Commitments as a framework to lead their team and help drive a high-performing culture.

• Monitor and coordinate the filling operations to ensure flawless execution and adherence to quality standards.
• Ensure the equipment and facility are cleaned and sanitized strictly following protocols.
• Lead and encourage a team to achieve production targets and maintain a collaborative and inclusive environment.
• Implement and uphold Baxter's Shared Commitments to drive a high-performance culture.
• Participate in continuous improvement initiatives, embracing and promoting a culture of ongoing development and learning.
• Apply Lean tools to streamline processes, reduce waste, and improve efficiency.

Safety and Quality

The top two priorities for all Baxter Alliston employees are Safety and Quality:

Safety: Support our goal to achieve a “Zero Harm Environment” by ensuring the safety of yourself and your coworkers through:

• Following all safety procedures.
• Understanding potential hazards in your area.
• Wearing appropriate PPE.
• Reporting all incidents, near-misses, and concerns.
• Embracing 6S principles.

Quality: Ensure the quality of our products to ensure patient safety and achieve our mission of “Saving and Sustaining Lives”. This can be achieved through:

• Following Good Manufacturing Practices (GMP).
• Adhering to all quality procedures.
• Completing training on time.
• Doing it Right the First Time.
• Reporting any quality concerns immediately.

Continuous Improvement

As part of the plant’s Enterprise Management System (EMS), all employees must embrace a culture of Continuous Improvement by:

• Participating in improvement activities.
• Identifying and implementing continuous improvement ideas.
• Participating in Tier meetings.
• Recognizing your peers.
• Embracing 6S.
• Identifying and implementing Value Improvement Projects (VIPs).
• Embracing continuous learning.
• Applying Leader Standard Work.
• Applying Root Cause Analysis tools to identify and prevent problems from recurring and drive measurable results.
• Participating and completing NCRs (Non-Conformance Reports) and CAPAs (Corrective and Preventive Actions).

Required Experience

• Experience within a manufacturing operation.
• Strong mechanical competence and ability to troubleshoot equipment.
• Practical experience using Lean tools (6S, LSW, VM, DA, Kaizen, Value Stream Mapping).

Preferred Experience

• Knowledge of GMP, ISO standards, and regulatory/corporate requirements.
• Previous supervisory experience within the pharmaceutical manufacturing industry.

Years of Experience

Required:

• 3 – 5 years of manufacturing experience.

Preferred:

• 5+ years of supervisory experience in a GMP regulated manufacturing facility.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

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