BAXTER: Manufacturing Supervisor

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.

Youll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxters 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.Summary The Supervisor I, Manufacturing is a member of the Manufacturing Leadership Team and reports directly to the Manufacturing Manager.

He or she provides direct support to Manufacturing personnel.

The Supervisor I, Manufacturing provides decision making and oversight to ensure compliance to all standard operating procedures and batch records.

He or she must communicate effectively with Manufacturing support departments (Quality, Technical Services, Engineering, etc.), multiple levels of management, and other customer support departments.

The Supervisor I, Manufacturing creates an environment where teamwork, productivity, safety, identity, strength, purity and quality (SISPQ) are reflected in the finished product.

This position reports to a Manager II, Manufacturing.

This position is on the overnight shift.

Essential Duties and Responsibilities (these are primary responsibilities of the role and the incumbent will perform other duties as assigned)Understand and follow current Good Manufacturing PracticesProvide guidance, support, direction and leadership through positive interactions with all personnel during daily operations.Interview, hire, coach, and develops staff.

Conduct annual performance reviews for all direct reports.

Assists in setting performance objectives and development plansSupervise the day-to-day production, scheduling, staffing, material management, compliance, training and auditing activities to meet customer requirements including deadlines and quality standards.Review, approve, and manage documentation for batch and system records.

Assist in release of product for distribution.

Assist in meeting product release time goals.Implement and support training programs designed to enable staff to consistently execute all manufacturing processes with strict compliance to cGMPs and EHS regulations.Develop and implement performance measurement and internal auditing programs in order to routinely evaluate operation efficiency and quality.

Implement changes as needed based on assessments.Perform/lead technical reviews, investigations and process improvement projects.

Provide manufacturing input into 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 audits and inspections.

QualificationsHigh School diploma or GED requiredBachelors degree preferredMinimum 2 years of manufacturing experience required, preferable in a cGMP environmentMinimum 1 year leadership experience requiredComputer proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software (examples include: JDE, BPLM, Pilgrim, Trackwise, etc.) Physical / Safety RequirementsAbility to stand or sit for extended periods of timeAbility to lift up to 50 poundsAbility to push/pull heavy wheeled objects (ie: tanks, carts, pallet jacks, etc.)Must be able to perform overhead work (ie: sanitizing walls and ceilings)Physical coordination/flexibility to allow gowning for clean room environmentsUtilize applicable personal protective equipment, including safety shoes/toe caps, gloves, eye protection, heat resistant wear and hearing protectionDexterity and physical condition to perform some level of repetitive motion tasksAbility to wear respirator usage when product or task requiresEyesight to ensure effective inspection of equipment and/or filled units (corrective lenses acceptable)Duties may require overtime work, including nights and weekendsUse of hands and fingers to manipulate office equipment is requiredMust be able to gown qualify for Grade A/B areas (filling) #IND-USOPS#LI-LH1Equal 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 LawEEO is the law Poster SupplementPay Transparency Policy Reasonable AccommodationsBaxter 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 NoticeBaxter 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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