Receiving inspection supervisor – queretaro siteabbott is building a manufacturing facility in querétaro, mexico.what you'll dovisual, dimensional, and functional inspection and testing according to documented policies and procedures.recording inspection and test data as prescribed by written instructions and procedures.operation of all associated test and measurement equipment.changes to related policies, procedures, and work instructions.processing non-conformances in the non-conforming material review system.acquisition of test and measurement equipment.provide daily supervision, work direction, and on-the-job training to receiving inspection staff.develops and maintains a competent work group through effective hiring, communications, recognition, performance feedback, and development.monitors, directs, and prioritizes staff workload to assure internal customer schedules are met.ensure all policies and processes are followed and monitor compliance with appropriate regulatory standards.contributes to establishing department goals, objectives, and accountabilities.contributes to developing and maintaining the department spending budget.recommends, justifies, and acquires measurement equipment and supplies to meet department objectives.advises on planning for department resource needs.supports monitoring inspection procedures for effectiveness.provides routine department status updates to management.effectively communicate with and provide support to other departments as necessary.motivate the team to achieve results.foster a department culture of continuous improvement.responsible to report quality issues immediately and co-lead their investigation, root cause analysis and solution.arrange reports to communicate backlog status, accomplishments and issues as required.
this may include leading daily meetings with staff to discuss issues and determine future actions that impact the inspection process.manage and report out quality metrics.make decisions on material disposition.education and experience you'll bringbachelor's degree in chemical sciences or industrial engineering.minimum 3 years related experience.certification in quality systems management.prior medical device experience preferred.experience as quality technical or supervisory roles is preferred.technical writing experience preferred.abbott is an equal opportunity employer, committed to employee diversity.
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