Detalle de la Oferta

Descripción de la Oferta

SUMMARY

Global support for supplier development and parts qualifications across Jabil Healthcare manufacturing locations. Ensures suppliers compliance with regulations and industry requirements. Assess supplier performance and risks as per Jabil's procedures.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.

- Ensure that all production critical supplier issues are resolved in a timely manner, and corrective actions are implemented correctly.
- Support component/part qualification and risk assessment program.
- Proactively communicate information or issues that may impact on the product costs of manufacturability to all affected departments.
- Provides regular updates to Supplier Quality Manager on the execution of the strategy.
- Technical escalation support in resolving supplier/component technical issues resulting in supplier corrective actions.
- Adherent to all safety and health rules and regulations associated with this position and as directed by supervisor.
- Provide support to all Safety, Health and Environment (EHS) programs and initiatives to support our zero-accident culture.
- Comply and follow all procedures within the company security policy.
- May perform other duties and responsibilities as assigned.

MINIMUM REQUIREMENTS

- Ability to use statistical analysis software such as Minitab would be preferred.
- Ability to work independently and with all stakeholders.
- Good communication skills in both Spanish and English languages.
- Be familiar with statistics tools and methods, FMEA/QCP, MSA, DOE, sampling plan, SPC, DMAIC/8D problem solving methodology, PPAP, Etc.
- Be familiar with Risk Assessments execution.
- Familiarity with SAP would be preferred.
- Team player, able to facilitate collaboration.

EDUCATION & EXPERIENCE REQUIRMENTS

- English proficiency (spoken and written).
- Bachelor's degree in business administration, Manufacturing, Industrial Engineering; preferred.
- At minimum of 0 to 2 years of experience in Supplier Quality (regulated industries preferred); or equivalent combination of education and experience.
- Proficiency in use of Microsoft Office products (Excel, Word, Power Point, Visio, and Project).
- Experience working in ISO / FDA regulated industry; preferred.

WORK CONDITIONS

- Regular business hours. Some additional hours may be required.
- Travel requirements: Domestic and/or Global, up to 30%.
- Climate controlled office environment during normal business hours.