Abbott
Healthcare
ProductionSupervisorIII
Neural analysis suggests this role is
optimal for Senior candidates.
“Production Supervisor III at Abbott. Skills: Production leadership, Quality systems, Process management. Assess and correct peers' completion of Supervisory responsibilities. Lead and support initiative to ensure regulatory compliance”
What You'll Achieve.
Deliver business results and expectations; Ensure safety, quality and production volumes are met; Accomplish production goals
Industry & Context.
Root cause analysis; Problem solving techniques
Work on different shifts schedule, Work in a clean room environment, Continuous sitting, Continuous standing, Continuous walking, Keyboard use
What They're Looking For.
Must Have
B. S. in Industrial Engineering, Administration or related field, 4-5 years supervisory experience, Computer skills, Proficiency on manufacturing systems, Knowledge of ISO and quality systems as FDA, MDD
Nice to Have
Supervisory experience in medical device, pharmaceutical, or electronic industry, Certification related or applicable to medical industry, Flexibility to work on different shifts schedule and areas, Capacity to effectively lead/influence peers and other functions, Knowledge of Costa Rica laws applicable to direct labor operators
What You'll Do.
Assess and correct peers' completion of Supervisory responsibilities
Lead and support initiative to ensure regulatory compliance
Report quality issues immediately
Co-lead investigation and solution of quality issues
Develop and execute plans to accomplish production goals
Maintain a safe environment
Analyze different systems to evaluate efficiency and compliance
Analyze production line leading indicators
Ensure adequate transition between shifts
Arrange reports to communicate production progress
Lead daily meetings with staff and peers
Discuss issues and determine future actions
Analyze daily production metrics
Establish mechanisms to ensure processes are in compliance
How You'll Work.
Team & Collaboration
Staff and peers; Other functions
Communication Scope
Arrange reports; Lead daily meetings
Full Job Description
## **JOB DESCRIPTION:** **Production Supervisor III** **About Abbott** Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. **Working at Abbott** At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to: * Career development with an international company where you can grow the career you dream of . * A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. * A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. **The Opportunity** This position works out of our Costa Rica – Alajuela location in the Structural Heart Division. Our business purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of structural heart disease. As the Production Supervisor III (NPIs), you will provide leadership to the production teams to deliver the business results and expectations on a day to day basis for one or more production areas. This position requires training in human resources/people skills, quality systems, and manufacturing processes. The position is responsible for ensuring that standard production processes are maintained and that safety, quality and production volumes are met. **What You’ll Do** • Assess and correct peers' completion of Supervisory responsibilities for production teams including personnel scheduling, evaluating discipline, coaching, selection and training of staff. • Lead and support any initiative to ensure regulatory compliance within all production areas with internal and external regulatory requirements (FDA, TUV, etc.). Re
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