Supervisor, Manufacturing
AbbottAbout the role
JOB DESCRIPTION:
A healthy heart is essential to good health. That's why we're committed to advancing treatments for people with cardiovascular disease. As a global leader in Cardiac Rhythm Technologies, our breakthrough medical technologies help restore people's health so they can get back to living their best lives, faster. We focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.
This position will be located in our Liberty, SC office.
THIS IS AN ONSITE POSITION.
Hours: 2nd Shift; 5:30pm - 3:30pm; Monday - Thursday
MAIN PURPOSE OF ROLE
The Manufacturing Supervisor will be responsible for driving the process of continuous improvement and lean principles. They are responsible for their shifts' performance with respect to safety, quality, on-time delivery and cost.
MAIN RESPONSIBILITIES
- Maintain high level of visibility with production staff. Use hands-on approach to communicate daily and involve production staff in problem solving.
- Develop a high performance work team with high levels of worker morale, satisfaction, and performance.
- Create and maintain a respectful work environment by listening, seeking facts to support decisions, managing one's own reactions, and addressing unacceptable behavior.
- Help production staff succeed through performance management. Provide coaching and performance communication to support development.
- Review general status of production schedules to identify and resolve problems.
- Ensure the desired product quality levels are achieved through use of standard work and training to those standards, training in operation and inspection techniques, and use of tools/data.
- Support and implement new, customer-focused processes in accordance with lean principles and practices. Provide training and coaching to improve standard work, work center organization (5S), and housekeeping. Actively provide change leadership as required.
- Support and foster an environment of continuous improvement by encouraging production staff to challenge existing processes and implement solutions that enhance the overall effectiveness of the operation.
- Support production staff in understanding company policies and practices.
- Maintain time and production records.
- Take notice of process related problems and support production staff in taking corrective action to improve the overall performance of the team.
- Communicate with and listen to production staff on a daily basis regarding work team performance, strategic initiatives, policy changes, safety, quality, etc.
- Communicate with other supervisors and appropriate personnel regarding equipment, safety, work center schedules, company policies and practices, performance improvement plans, etc.
- Hires and retains a diverse, highly qualified staff and provides ongoing performance feedback. Maintains a safe and professional work environment.
- Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements
- Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
QUALIFICATIONS
Education
- Associates Degree (± 13 years) preferred or an equivalent combination of education and work experience
- Bachelors Degree (± 16 years) preferred or an equivalent combination of education and work experience
Experience/Background
- Minimum 3 years
- Previous experience in manufacturing operations with demonstrated ability to acquire and apply manufacturing principals is preferred.
- Experience working in a broader enterprise/cross division business unit model preferred. Ability to work in a highly matrixe
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