Supv I, Manufacturing
Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-center dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter’s employees worldwide are building upon the company’s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care.1) Supervise the daily manufacturing operations in an area ? maintain (audit, refine, improve) equipment and processes within this area. 2) Provide a positive and equitable working environment emphasizing the Baxter Shared Values ? Respect, Responsiveness and Results. 3) Support and Emphasize the Safety and Quality commitments of the department ? make decisions concerning these commitments within the area. 4) Ability to utilize resources and raw materials in the most efficient and productive manner possible. 5) Identify/prioritize/provide resources in an area to assist the superintendent to meet the annual operational plan and budgetary commitments, 6) Facilitate and verify appropriate training for employees in the area (including but not limited to GMP, job skills, safety) 7) Ensure compliance with all GMP rules, product documentation, specifications, SOPs, and FDA requirements as required. 8) Commit to employee feedback and developmental process ? support Talent Management goals, conduct recognition and disciplinary action for employees, facilitate employee representation throughout the organization. 9) Submit and/or maintain and distribute reports related to attendance, labor, efficiency, safety, scrap and others as needed. 10) Ability to utilize resources and raw materials in the most efficient and productive manner possible. 1) Demonstrated interpersonal and leadership skills with ability to interface well with other departments, and lead effectively and efficiently in a team environment. 2) Ability to manage multiple priorities in a manufacturing plant setting. 3) Strong professional writing skills and ability to prepare technical reports. 4) Ability to understand GMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry. 5) Strong assessment and troubleshooting skills. 6) Good computer skills. 7) Interact with all levels of personnel to analyze and solve problems related to manufacturing, Quality, documentation, and personnel issues.) 8) Work in and facilitate a team-oriented environment. 9) Collect and analyze data and information to determine paths for process improvement and potential root cause/corrective actions in the case of exceptions.� 10) Ability to respond to detailed inquiries, and present information to groups and senior management. 11) May be required to supervise multiple groups. 12) BS degree in a scientific or engineering discipline with 0-3 years of manufacturing experience or equivalent manufacturing experience.
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.
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an email to Corporate_Staffing_Deerfield@baxter.com or call 877-229-4748 (877-BaxHR4U) and let us know the nature of your request along with your contact information.