Manufacturing Supervisor II - 1st Shift

This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride.

Baxter Healthcare Corporation encourages team members to reach their full potential. In the role of Manufacturing Supervisor II, you will contribute significantly to producing high-quality healthcare products accurately and efficiently. This position allows you to lead and cultivate a motivated team in a dynamic environment, ensuring smooth operations that meet rigorous quality standards.

• Communicate guidance, support, direction, and leadership through effective interactions with all personnel during daily operations.
• Supervise day-to-day production, scheduling, staffing, material management, compliance, training, and auditing activities. Identify, prioritize, and provide resources as appropriate.
• Interview, hire, coach, motivate, develop, recognize, and manage the performance of direct reports. Provide regular feedback to all direct reports. Assist in setting performance objectives and development plans and supervise progress.
• Review, approve, and lead documentation for batch and system records. Assist in the release of products for distribution and meeting product release time goals.
• Identify, initiate, and facilitate continuous improvements, lean manufacturing activities, and initiatives like 5S, visual management, and kaizens. Identify and implement VIPs.
• Ensure resources and raw materials are applied in the most efficient and productive manner possible.
• Develop training content and facilitate and verify appropriate training assignment and completion for employees in the area.
• Ensure compliance with all GMP rules, product documentation, specifications, SOPs, and FDA requirements as required.
• Submit and/or maintain and distribute reports related to attendance, labor, efficiency, safety, scrap, and others as needed.
• Perform/lead technical reviews, investigations, and process improvement projects.
• Provide manufacturing insights for the integration and validation of new equipment and processes.
• Resolve technical, material, and cGMP problems that may impact project deadlines. Provide guidance and troubleshooting assistance as needed during a deviation in the process.
• Represent the company during FDA inspections or provide information as necessary to FDA that establishes credibility and demonstrates compliance with cGMPs.
• Monitor capital expenditures and assist in developing budgets.
• Learn, understand, and apply rigorous quality standards, established guidelines, and current Good Manufacturing Practices (cGMP).
• Notify the supervisor and take appropriate action if any safety, quality, mechanical, or discrepancy issues occur.
• Sustain a clean and safe work area using 6S principles.

• Proven track record of interpersonal and leadership skills with the ability to lead, coach, motivate, and enforce company policy and standard operating systems.
• Ability to interface well and collaborate with other departments while leading effectively in a team environment.
• Comprehensive understanding of associated manufacturing machinery and procedures.
• Ability to manage multiple priorities in a high-paced manufacturing plant setting.
• Strong professional writing skills and capability to prepare technical reports. Ability to clearly communicate information during regulatory/client inspections.
• Understanding of GMPs and other applicable regulatory guidelines.
• Strong assessment and troubleshooting skills.
• Ability to respond to detailed…