Supervisor de Produccion, Manufactura
cardinal health
Alajuela, Alajuela, Costa Rica
hace 7 horas

What the Production Supervisor contributes to Cardinal Health

Manage the coordination of departmental functions to ensure business unit realization of safety, quality, service, and financial objectives.

This includes leading hourly associates while working closely with others through mutually supportive contributions and effective interactions.

Accountabilities

Work closely with all members of the business unit to ensure that business unit objectives are exceeded. This includes working with the business unit leadership team in setting priorities and properly deploying resources.

Demonstrate a clear understanding of regulatory requirements and of GMP standards through compliance of the Divisional Quality policy.

Develop cooperation and teamwork while leading a diverse group of people, working towards solutions which balance business, customer, and associate needs.

This includes an ability to work with others easily, establishing a climate of trust, confidence, and mutual respect.

Demonstrate concern for meeting internal and external customers’ needs in a manner that provides customer satisfaction through the effective use of resources.

Strive to improve the skills of associates by providing clear performance expectations, specific feedback on behaviors, effective coaching and mentoring, identifying and providing developmental opportunities, and accurate, timely performance appraisals.

Demonstrate a commitment to Operational Excellence through fostering and promoting an environment of continuous improvement.

Use appropriate interpersonal styles and methods to gain agreement or acceptance of the Safety principles.

As a leader and a salaried representative of the Management Team you are expected to be a role model in exhibiting the behaviors and fostering the development of Integrity, Excellence, Teamwork, and Accountability.

Qualifications (minimum requirements)

Bachelor’s degree in Chemistry, Engineering, or related scientific field is required. MBA is preferred

3+ years’ experience on medical devices or similar regulated manufacturing environment including supervision of a team

Advance proficiency in English

Knowledge of GMP

Knowledge of FDA Quality System Regulations and ISO Quality Systems requirements

SPC knowledge

Validation experience and Inventory management

Proven track record of process improvement and lean manufacturing

Excellent computer skills, proficiency in MS Office suite, 4M and Minitab

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