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Production Filling Supervisor

3 months ago


Alliston, Ontario, Canada Baxter Full time

Make a difference in healthcare

At Baxter, our mission is at the heart of everything we do. Each role contributes to a greater purpose, positively impacting patients' lives globally. You will experience a profound sense of fulfillment as your efforts enhance healthcare outcomes for millions.

With over 85 years of pioneering medical innovations, Baxter's products and therapies are integral to hospitals, clinics, and homes worldwide.

We foster an environment where success is shared, and inspiration flows. This is where you can truly excel.

As a Filling Supervisor, you will oversee the filling of high-volume IV solutions utilizing advanced automated machinery. Your role involves monitoring team performance and machinery operations to ensure optimal product output while adhering to quality standards and cost-efficiency. Additionally, you will be responsible for maintaining cleanliness and sanitation in the work area.

Key Responsibilities

Enhance team performance through structured training, coaching during feedback sessions, and daily guidance to develop skills, while recognizing exemplary contributions. Ensure fair and consistent application of company policies, addressing any unacceptable behaviors promptly. Set up, adjust, troubleshoot, and repair automated equipment on the production line. Provide technical assistance to staff to resolve quality and equipment challenges. Participate in and complete Non-Conformance Reports (NCRs) and Corrective and Preventive Actions (CAPAs). Identify and implement Value Improvement Projects aimed at reducing costs or enhancing quality by monitoring waste and efficiencies, discussing outcomes with team members, and applying innovative ideas to refine processes. Guarantee compliance with specifications and Good Manufacturing Practices (GMP) by reviewing batch records, taking corrective actions for deviations, and implementing preventive measures against non-conformances. Maintain the facility and equipment to meet all GMP and 6S standards. Achieve financial objectives by ensuring adherence to budgeted labor standards throughout the year and assisting in the development of departmental budgets and production standards for the upcoming year.

Educational Requirements

Required:

Completion of High School or GED

Preferred:

Post-Secondary education

Required Skills and Experience

Required:

Experience in a manufacturing environment Strong mechanical aptitude and troubleshooting skills. Practical experience with Lean methodologies (6S, LSW, VM, DA, Kaizen, Value Stream Mapping).

Preferred:

Familiarity with GMP, ISO standards, and regulatory requirements. Previous supervisory experience in pharmaceutical manufacturing.

Experience Level

Required:

3 – 5 years in manufacturing roles.

Preferred:

5+ years of supervisory experience in a GMP-compliant manufacturing setting.

Additional Skills

Required:

Experience in people management, coaching, and team development. Excellent communication skills, capable of engaging with all organizational levels. Ability to manage multiple priorities in a dynamic, high-pressure environment. Self-driven with a proactive approach to continuous improvement aimed at cost reduction and quality enhancement. Strong analytical, problem-solving, and critical thinking capabilities. Intermediate proficiency in Word, Excel, PowerPoint, and Electronic Batch Records (EBR). Solid understanding of SOPs, specifications, blueprints, Process Control Systems (PCS), and Bills of Materials (BOM).

Preferred:

Knowledge of APF, Manual Fill, Rovema, Pouch Sealing, and Truck Loader operations.

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