Manufacturing Supervisor II

Your role as a Manufacturing Supervisor II, positions you to be directly involved in the physical production that enables Baxter to fulfill our mission to save and sustain lives. You own the line between meeting production timelines and making quality products. As a manager, you are the trusted critical connection between the business and the workers on the floor.

You will lead and oversee daily operations within a designated production area to ensure manufacturing goals, productivity targets, and project timelines are achieved. You will ensure compliance with current Good Manufacturing Practices (GMP), Environmental Health and Safety (EHS) standards, and all applicable regulatory requirements. You will coordinate resources, support workforce performance, and help drive operational excellence, quality, safety, and efficiency across the production environment.

Shift: You will work a 12-hour night shift from 6:00 PM to 6:00 AM on a rotating 2-2-3 schedule. This two-week cycle includes every other weekend and follows this pattern: work 2 days, off 2 days, work 3 days, off 2 days, work 2 days, and off 3 days.

Your Team

Baxter is focused on saving and sustaining lives by finding solutions to sophisticated problems. Each day, the manufacturing team strives to create quality products for our customers—and are sometimes met with unforeseen issues to solve. The high-caliber talent at Baxter meets these challenges head-on, as a team, to create products with the customer's needs top-of-mind.

We establish relationships with each other to get work done.

As a multidisciplinary environment, we are always learning from others and exchanging ideas. This means we are open to new opinions and encourage Baxter employees always to be their authentic selves and celebrate our various backgrounds.

Our manufacturing facility is a high-energy environment with little downtime. We have robust processes that ensure our employees are safe and healthy—both mentally and physically. We pride ourselves on being top of the line regarding cleanliness and safety.

as required.

• ✓Performs/leads technical reviews, investigations and process improvement projects.
• ✓Provides manufacturing input into integration and validation of new equipment and processes.
• ✓Resolves technical, material and cGMP problems that may impact project deadlines. Provides guidance and troubleshooting assistance as needed during a deviation in the process.
• ✓May represent the company during FDA inspections or provide information as vital to FDA that establishes credibility and demonstrates compliance with cGMPs.
• ✓May monitor capital expenditures and assist in developing budgets.
• ✓Submit and/or maintain and distribute reports related to attendance, labor, maintenance metrics, safety, and others as needed.
• ✓Sustain a clean and safe work area using 6S principles
• ✓Learn, understand and apply rigorous quality standards, Standard Operating Procedures (SOPs) and Current Good Manufacturing Practices (cGMP)