Sr. Manufacturing Supervisor - 2nd Shift

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.
Your Role at Baxter

This is where we make life-saving products
You will supervise daily activities in the production area to ensure manufacturing goals and project deadlines are met while maintaining compliance with current good manufacturing practices (cGMPs), SOPs, environmental health and safety (EHS) guidelines and any other regulations that may apply. Monitor and insure efficiency and effectiveness in various areas. Ensure operational efficiency, troubleshoot and investigate as vital. Perform all duties with a focus on optimizing safety, quality, service and cost. May supervise more than one department.
Your role as a Supervisor positions you to be directly involved in the physical production that enables Baxter to fulfill our mission to save and sustain lives. You will manage 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.

Your Team

Baxter is passionate about saving and sustaining lives by finding solutions to complex problems. Each day, the manufacturing team strives to create quality products for our customers—and are sometimes met with unforeseen issues to tackle. 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.

What we offer from Day One
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

What you will be doing:
Total compliance with all applicable specifications, SOPs, FDA regulations (GMPs) and new drug applications.

Technical expertise and direction are provided to all quality and manufacturing operations in order to facilitate successful completion of routine tasks, as well as, product/process improvements and problem solving.

Must interface with various support departments such as QM, Engineering, Maintenance, Scheduling, Accounting, and Human Resources.

Responsible for adequacy of Specifications and SOPs to assure all products meet the requirements for quality, safety, and integrity.

Improve quality and reduce customer complaints through a proactive program that includes interaction with internal and external suppliers to improve quality of incoming materials and utilize collective data from customers to enhance quality of the product, as perceived by the customer.

Plan, develop and manage shift teams that monitor, predict or regulate all steps of manufacturing.

These activities are accomplished through statistical sampling, product auditing and process control.

Assist in the validation of new equipment, process, systems, and changes that impact product quality.

Represent the company during FDA inspections.

Provide information as necessary to FDA that established creditability and demonstrated compliance with GMPs.

Review, approve, and manage documentation for batch and system records.

Assist in the release for distribution.

Assist in meeting product release time goals.

Create an environment that stresses and encourages teamwork.

Support and encourage all plant activities, i.e., VIPs, QLP, CIs, TPM, Business Process teams Supervise Injection/Husky/LSR operations and staff. Payroll, Production input and reviews. Conversion loss reduction.

Responsible for Quality, Production and overall operating performance of the assigned shifts.

Will have knowledge of both plant and department environmental health and safety regulations and comply with said regulations accordingly.

Will manage multiple shifts and/or multiple departments

Will perform all other duties and responsibilities as determined by supervision/management.

What you will bring:
Bachelor's degree preferred; minimum Associates degree required, with technical discipline preferred.

3 years or more manufacturing and Plastic injection molding experience highly desirable and 2 years or more of supervisory experience

Substantial interpersonal skills both verbal and written for interaction with plant management and subordinates.

Computer skills to include Word, Excel, PP and JDE.

Lean six sigma training/green belt desirable.

Audiometric testing required and hearing protection required.

Ability to stand for long periods of time.

Ability to work occasional off shifts to monitor work performance and meetings.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $72,000.00 - $99,000.00 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.
#LI-BAXGEN
The successful candidate for this job may be required to verify that he or she has been vaccinated against COVID-19, subject to reasonable accommodations for individuals with medical conditions or religious beliefs that prevent vaccination, and in accordance with applicable law.
Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

EEO is the Law
EEO is the law - Poster Supplement
Pay Transparency Policy
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

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our

Recruitment Fraud Notice .
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