GE HealthCare Production Associate Group Leader 

United States, Arizona, Phoenix 

831383486

The Production Associate Group Leader is responsible for directing the day-to-day work in the assigned area. They may provide input or recommendations to supervisory personnel on hiring, performance assessment and discipline. They are responsible for execution of the daily, weekly and monthly forecasted production priorities required to meet output quotas and group performance goals.

Key Responsibilities:

• 2nd Shift Position: 1:30pm-10:30pm, Mon-Fri
• Reads work procedures and schematics, and provides instruction to others when required
• Strive to be trained in as many operations within assigned area as possible.
• Audit that workstation is maintained according to 5S and that required tools are available and in good working order and escalate if additional action is required
• Monitoring the daily production flow and adjusting workload and resources appropriately in assigned area.
• Follow up on defects being reported and handed over to rework area according to defined routine. Escalate and report reoccurring defects in Tier 2.
• Respond to alerts from assigned area
• Making sure defined area has correct amount of material available at all time and supply when necessary.
• Assisting in implementation of process improvements to increase quality and productivity levels
• Monitoring and escalating QA/RA and EHS procedures and policies as required
• Ensuring manufacturing documentation used during the production process is of the correct and most current revision

Quality Specific Goals:

• Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position
• Complete all planned Quality & Compliance training within the defined deadlines
• Identify and report any quality or compliance concerns and take immediate corrective action as required
• Training: Aware of and comply with GEHC training requirements
• Knowledge and understanding of production process, work instructions, documentation configuration control, non-conforming & rework documentation requirements and operates within them to ensure that a device conforms to it’s specification.
• Aware of and comply with Stop Order, Concessions, ESD, Calibration, Preventative Maintenance, Material Identification & Segregation, and Good Documentation Practices, as associated with this job type/position

Required Qualifications:

• High School Diploma or local equivalent
• 5 or more years of related manufacturing experience
• Ability to communicate, receive and understand instructions regarding duties to be performed
• Ability to provide instructions regarding policies and procedures

• Preferred Qualifications:

• Associates degree or local equivalent
• Prior management experience
• Prior experience working in a medical device manufacturing environment
• Previous experience in GMP work environment
• Take lead in different projects and/or specific tasks as needed in addition to regular tasks described herewith.
• Other duties as assigned, and may be asked to be included in quality activities, training sessions, and employee activity teams
• Participates in quality control inspections when required
• Comply with EHS regulations and policies