Production Supervisor II
Abbott Laboratories
Localização do trabalho
Alajuela Province, Alajuela
Status de emprego
Tempo total
Detalhes sobre a oferta de trabalho
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
• Consistently fulfills his/her Supervisory responsibilities for production teams including personnel scheduling, evaluating discipline, coaching, selection and training of staff by constant presence in the line.
• Coordinate and provide help to ensure own production lines and related areas regulatory compliance to internal and external regulatory requirements (FDA, TUV, etc.). Responsible to report quality issues immediately and be closely involved in their investigation and solution.
• Analyze and propose 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. This includes proper application of systems to evaluate the state of efficiency and compliance of his/her area of production.
• Prepare and review prod line leading indicators with prior or following supervisor to ensure that the transition between shifts is adequate.
• Prepare standards reports to communicate production progress, accomplishments and issues on a frequent basis.
• This may include leading and daily meetings with staff and peers to discuss issues and determine future production schedules. Evaluates and validates daily production metrics and establishes mechanisms to ensure that all processes are in compliance with standard procedures.
• Employee performance/engagement Supervise and train (organize, plan, direct and control) his/her production teams to achieve the expected quality, production schedule, staffing and safety goals. Analyze and propose different initiatives to motivate and energize personnel to obtain top performance. Ensures adequate communication to staff of all required HR related information.
• Shift C
Required Qualifications
• B.S. in Industrial Engineering, Administration or related field.
• 1-3 years supervisory experience. Preferably in a medical device, pharmaceutical, or electronic industry.
• Intermediate command of English.
• 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.
• Shift C
Preferred Qualifications
• Knowledge of Costa Rica laws applicable to direct labor operators is a plus.
Apply Now
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal
