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Balt · 4 hours ago

Production Supervisor 1st Shift

Irvine, California, United States

Full-time

Onsite

Entry, Mid Level

$90K/yr - $100K/yr

2+ years exp

Balt is a rapidly growing pioneer in the medical device industry, dedicated to improving the lives of patients. The Production Supervisor will be responsible for overseeing manufacturing operations, ensuring compliance with quality standards, and leading a team to meet production objectives.

Health CareManufacturingMedical Device

Responsibilities

Coordinates the day-to-day activities of a team of quality and production personnel to ensure that manufacturing operations run according to established production specifications and schedules, volume, cost and quality standards

Monitors the quality and volume of output and adjusts tasks, timing, equipment set-up or inputs so that production specifications are met, and resources are used efficiently

Supervises staff to ensure that all quality and production tasks are performed, and all machines and equipment operated safely

Trains new workers in the organization's operating procedures and standards

Provides quality information for manufacturing by compiling, initiating, sorting, and analyzing production performance records and data, answering questions and responding to requests

Perform regular daily audits of key processes to ensure optimum process performance

Ensures production is performed in full compliance with the Quality System and all procedural requirements

Ensure fair and consistent application of company and departmental policies and practices. Works with personnel to resolve employee relations issues and concerns; involves HR when needed

Actively participates and supports continuous improvement activities

Leads activities to communicate and maintain adherence to company policies, quality standards, safety standards, and good manufacturing practices

Provide ongoing feedback and mentoring of Quality and Manufacturing personnel, including writing and delivery of annual performance reviews

Support investigations associated with non-conformances

Work with engineers to determine appropriate support activities for non-conforming goods and new products

Interface with the FDA, state agencies, and notified bodies during certification, surveillance and routine ISO audits

Participate in cross-functional Quality Objective teams

Support inventory counts by owning Work Order Open/Closing on ERP system

Qualification

Quality SystemsSix Sigma/Lean toolsMechanical drawingsMicrosoft OfficeIntra-personal skillsDelegateCommunication skillsOrganizational skillsLeadership abilitiesConflict resolution