Production Supervisor Iii - Alajuela, Costa Rica - Abbott Laboratories

Abbott Laboratories

Empresa verificada

Alajuela, Costa Rica

hace 1 semana

Publicado por:

Andrea Rodríguez

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Descripción

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 Electrophysiology Division.

In Abbott's Electrophysiology (EP) business, we're advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.

As the Production Supervisor, 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.). Responsible to report quality issues immediately and colead their investigation and solution.
Develop and execute plans to accomplish the production goals, which include productivity indicators, schedule adherence, quality, cost and service while maintaining a safe environment. Have full responsibility / ownership of his/her area of production and related areas as gowning, clean corridors, etc. This includes analyzing different systems to evaluate the state of efficiency and compliance of his/her area of production and related areas.
Analyze production line leading indicators with prior or following supervisor to ensure that the transition between shifts is adequate.
Arrange reports to communicate production progress, accomplishments and issues as required. This may include leading daily meetings with staff and peers to discuss issues and determine future actions that impact overall production line. Analyses daily production metrics and establishes mechanisms to ensure that all processes are in compliance with standard procedures.

Required Qualifications

B.S. in Industrial Engineering, Administration or related field.
45 years supervisory experience. Preferably in a medical device, pharmaceutical, or electronic industry.
Computer skills.
Demonstrated proficiency on manufacturing systems used to collect data and control/monitor processes. For example SFA, SAP, Kronos, or similar.
Demonstrated knowledge of ISO and quality systems as FDA, MDD.
Desirable at least one certification related or applicable to medical industry. For example, CQE, 6Sigma black belt, lean coach, problem solving techniques, etc.
Flexibility to work on different shifts schedule and areas is preferred.
Demonstrated capacity to effectively lead/influence peers and other functions towards organizational goals.
Intermediate Command of English.

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SHIFT C:
Monday - Friday: 10:00pm to 6:00am

Preferred Qualifications