Supervisor de Manufactura at Baxter International Inc.

Cartago, , Costa Rica -

Full Time

Start Date

Immediate

Expiry Date

12 Jun, 26

Salary

0.0

Posted On

14 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Process Control, Inventory Oversight, Accident Prevention, GMP Compliance, FDA Regulations, ISO 9001, ISO 14001, OHSAS 18001, Personnel Development, Continuous Improvement, Lean Six Sigma, DMAIC Methodology, Kaizen Events, Value Stream Mapping, English Language, Computer Systems Management

Industry

Medical Equipment Manufacturing

Description

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. Are you ready for your next Challenge? This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role, 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 90 years, we have pioneered significant medical innovations that transform healthcare. Together, we build a place where we are happy, successful, and encourage 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. You role at Baxter: Supervise activities at Baxter-Cartago plant, ensuring compliance with build requirements, specifications, and procedures. You will have the task of Supervisor Indicators of your areas and participate in the identification of GMP, as well as in the establishment and implementation of containment, corrective and preventive actions when applicable. #this is where your creativity addresses challenges! Your Team: Within Supervisor, every role makes a difference. Products that Baxter makes are shipped worldwide for patients in need. Supervisor team members have the opportunity to develop new processes and tackle outstanding production issues. Every contributor at Baxter touch a portion of our global operation. What you'll be doing : Ensure high standards of process control (good process indicators, accurate oversight of inventories of materials used in the production process, orientation to accident prevention, DPM's, complaints and others) 2. Uphold a safe work environment, consistently adhering to the company's principles and encouraging a collaborative work atmosphere. 3. Support and compliance in the application of the guidelines related to good manufacturing practices "GMP'S", regulations established by FDA / ISO 9001 / ISO 14001 / OHSAS 18001 and other regulations and policies of the company (SOX, 6'S etc). 4. Empower, develop, attract the best personnel in your area. 5. People with backgrounds other than that of engineer may work in the position, as long as the suitability of the person for the position they are going to perform is confirmed with facts. There may also be training plans for the leveling of the person's knowledge, a decision that will be made by the director of the area. 6. Own the personnel under their responsibility with good success. 7. Promote continuous improvement initiatives in the areas under its responsibility, incorporating the appropriate application of modern engineering tools and concepts (Lean six sigma, DMAIC methodology, Kaizen events, Value Stream Mapping, Poke Yoke, Kanban, JIT, Ishikawas, FMEA, and others) for the reduction of waste. 8. Ensure adequate compliance with the production plans in terms of mix and volume established by the planning area. 9. Ensure continuity in the flow of the finished product, seeking to resolve situations that interrupt it in time. 10. Ensure compliance with the regulatory training needs of the personnel under their charge. 11. Provide support in the strategy of work teams developed in the plant (Cells/Cells/SLTs), promoting teamwork and facilitating the processes of involvement of personnel. 12. Coordination with other functional areas to promote the execution of initiatives and projects in the areas under its responsibility. What you'll bring to the table !! Intermediate/advanced level of the English language. Management of computer systems (Office). Knowledge of Quality Systems (FDA, GMP's, ISO 9001 regulations, among others). 3-5 years of experience in supervision Availability to work in shifts B 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. 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. No matter your role at Baxter, your talent, skills, and time has a direct impact on people's lives. Since 1931, we have been at the forefront of innovation by bringing smarter, more personalized care to patients around the world. Now, we're more determined than ever to make a lasting impact as we are redefining healthcare delivery across the care journey. Our Mission to Save and Sustain Lives motivates us as we create a culture in which each of us can succeed. This is where you belong.

Responsibilities

The supervisor will oversee activities at the Baxter-Cartago plant, ensuring adherence to build requirements, specifications, and procedures while managing area indicators and participating in GMP identification and corrective actions. Key duties include maintaining high standards of process control, upholding a safe work environment, and promoting continuous improvement initiatives using modern engineering tools.