Production Associate Group Leader

GE HealthCare; Phoenix (AZ); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading company in medical technology is seeking a Production Associate Group Leader in Phoenix, Arizona. This role involves directing production activities, ensuring quality compliance, and leading a team to meet performance goals. The ideal candidate will have significant manufacturing experience and strong leadership skills, contributing to a collaborative and efficient work environment.

Benefits

Professional development opportunities

Competitive compensation

Qualifications

• 5 or more years of related manufacturing experience.
• Ability to communicate and provide instructions regarding policies and procedures.
• Knowledge of production processes and compliance requirements.

Responsibilities

• Direct day-to-day work in the assigned area and monitor production flow.
• Ensure compliance with quality and safety standards.
• Assist in implementation of process improvements.

Skills

Communication

Leadership

Quality Assurance

Education

High School Diploma or local equivalent

Associates degree or local equivalent

Job description

Job Description Summary

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.

Job Description

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
• Participatesinqualitycontrolinspections when required
• Comply with EHS regulations and policies

Additional Information

GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is anEqual Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).

While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees.

Relocation Assistance Provided: No