GE HealthCare Production Team Leader United States, New York, City of Troy 181837016
Provide clear direction and leadership to a team of skilled Technicians
Conduct employee performance reviews, set individual and team goals, and deliver ongoing coaching to enhance development, engagement, and performance.
Ensure timely material procurement and accurate production forecasting based on deliverable needs; monitor time-sensitive materials closely
Monitor and improve productivity while ensuring customer commitments are met with high quality, timeliness, and cost efficiency.
Plan and execute production tasks to optimize tool utilization and labor efficiency, maximizing throughput
Lead and support documentation activities related to medical device manufacturing, ensuring compliance with regulatory requirements
Develop and implement training plans to build workforce capability and flexibility
Lead compliance and Environmental, Health & Safety (EHS) initiatives in alignment with plant goals
Drive implementation of LEAN manufacturing practices to improve operational efficiency
Communicate with material and tool vendors as needed to coordinate maintenance and servicing in collaboration with the engineering team
Coordinate process flow for Device History Records (DHRs), manage data within electronic record systems, and oversee tool maintenance schedules
Manage P&PC change control procedures in partnership with engineering for changes impacting process qualification or production toolsets
Execute business unit objectives and manufacturing department goals across all functional areas
Perform other duties as assigned
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
Maintaining full Quality System Regulation and Current Good Manufacturing Practices requirements
Maintaining full regulatory compliance and other legal requirements
Knowledge and understanding of production process Work Instructions and operates within them to ensure that a device conforms to its specifications
Ensures the creation of accurate, complete, and timely records and DHRs
Bachelor’s Degree in an engineering or technical discipline and 2 years semi-conductor manufacturing, supply chain, or leadership experience, or Associate’s Degree in an engineering or technical discipline and 4 years semi-conductor, supply chain experience, or leadership experience, or HS Diploma/GED with 6 years semi-conductor manufacturing, supply chain, or leadership experience
Demonstrated ability to lead and develop teams.
Strong mechanical aptitude and experience running critical manufacturing tool sets
Demonstrated ability to implement and qualify processes and procedures within a regulated industry
Excellent oral and written communications skills to employees at all levels of an organization
Demonstrated ability to identify and implement best practices and deal with high levels of ambiguity
Demonstrated ability to operate independently and exercise good discretion, troubleshooting, and decision-making
Prior team leading or supervisory experience
High proficiency to interpret, instruct, and explain complex technical information
Fast learner with ability to synthesize data and draw conclusions accordingly
Familiarity and experience with Quality Management Systems in an FDA regulated environment
Six Sigma certified
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