Manufacturing Supervisor, II (12-Hour Nights) Job at Baxter (Round Lake)

Job Description

This is where we make life-saving products. You have deep knowledge of and experience with manufacturing processes. You understand the importance of forming relationships, establishing order, and maintaining clear communication channels. As a Manufacturing Supervisor II, you are a leader who is willing to listen and inspire others by your actions. You also appreciate the stability of a large multinational company with a long history of growth and success. Your team is an extension of your family, and you know how to support them as individuals while helping them achieve results as a team. 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.

Job Responsibility

Communicates guidance, support, direction and leadership through effective interactions with all personnel during daily operations
Supervises the day-to-day production, scheduling, staffing, material management, compliance, training and auditing activities
Identify/prioritize/provide resources as appropriate
Interviews, hires, coaches, motivates, develops, recognizes and leads performance of direct reports
Provides regular feedback to all direct reports
Assist in setting performance objectives and development plans and supervise progress
Reviews, approves, and handles documentation for batch and system records
Assists in release of product for distribution
Assists in meeting product release time goals
Identifies, initiates and facilitates continuous improvements, lean manufacturing activities and initiatives, such as 5S, visual management, kaizens
This role may also be responsible for identifying and implementing VIPs
Insures resources and raw materials are applied in the most efficient and productive
Develops training content and facilitates and verifies appropriate training for employees in the area
Ensures compliance with all GMP rules, product documentation, specifications, SOPs, and FDA requirements 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)

Requirements

Bachelors degree in Business, Engineering, related field or equivalent, is required
3 years manufacturing experience
2 years of Supervisory experience
A candidate must not be allergic to Penicillin and Cephalosporin or their related products and minerals
Demonstrated communication, administrative and strong technical leadership skills with ability to interface well with other departments and lead effectively and efficiently in a team environment
Solid professional writing skills
Ability to lead multiple priorities in a manufacturing plant setting
Good assessment and troubleshooting skills (mechanical, electrical, and process) with demonstrated and confirmed experience and background
Proven understanding of maintenance systems to include preventive maintenance and CMMS
Ability to understand regulatory and safety guidelines applicable to the medical / pharmaceutical industry and industry in general
Must have experience and knowledge with Lockout / Tagout and other Safety Programs
Interact with all levels of personnel to analyze and solve problems related to equipment but also with manufacturing, quality, engineering, and personnel issues
Knowledge of WCM methods (Lean, Six Sigma, and QLP)
Ability to respond to detailed inquiries, and present information to groups and department management
Have good project management skills and ability to organize many projects and priorities as required
Understand verbal and written safety and quality instructions and read and comprehend written work instructions including words and drawings
Must have basic English written and oral communication skills adequate to communicate with other team members

What we offer

Medical, Dental and Vision coverage
160 hours of Paid Time Off and Paid Holidays
401K match
Employee Stock Purchase Program
Paid Parental Leave
Tuition Reimbursement

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Manufacturing Supervisor, II (12-Hour Nights)

Job Description

Job Responsibility

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