We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further — Haemonetics is your employer of choice.
The Production Supervisor for Haemonetics Plasma products manufacturing is responsible for managing assigned production area and staff and workflow to consistently meet or exceed production schedules, delivering the highest quality product, whilst ensuring the safety of all personnel on shift. Night Shift Position working Mon-Fri Schedule (10:30pm – 7:00am)
ESSENTIAL RESPONSIBILITIES:
Productivity/Output
Accountable for ensuring that production schedules are met on a daily/weekly/quarterly basis.
Supervises direct labor production employees, which may include Group Leaders, Machine Operators, Assembly Specialists, Production Operators, Technicians, Material Handlers and Material Coordinators.
Monitors, manages and reports on key production metrics for assigned shifts/lines/areas of responsibility on daily/weekly/monthly/quarterly basis.
Directs the entry of select transactions (high dollar inventory adjustments, inventory adjustments, high scrap values) into Oracle/SAP. (Braintree, not SLC, Ascoli done by warehouse employees, Bothwell done by )
Develops and implements continuous improvement projects across shifts/lines/areas of responsibility.
Accountable for ensuring actions relating to Continuous Improvement projects are implemented within production line or area.
Identifies and eliminates reasons for chronic part shortages or root-cause production slowdowns.
Quality
Accountable for ensuring that production output meets established quality standards on a daily/weekly/quarterly basis.
Accountable for ensuring that production processes and employees comply with regulatory standards (FDA, cGMP, ISO13485, MDD and Country-Region regulations).
Monitors, manages and reports on quality metrics for assigned shifts/lines/areas of responsibility on daily/weekly/monthly/quarterly basis or as appropriate.
Develops and maintains monitoring systems that improve visibility of key production metrics such as in-process defects, scrap and in-process inventory.
Ensures that Quality Management System (MI’s, SI’s, Training Records) procedures accurately reflect production processes.
Accountable for process deviation corrective action. Initiates and completes containment and lot tracing, closes out NCE's
Safety
Accountable for the health and safety of all assigned work areas and personnel.
Ensures safety regulations are understood and followed by all assigned staff and implementing safety related disciplinary actions as needed.
Ensures that production process and employees comply with all relevant health & safety regulatory standards.
Supports the investigation of H&S accidents and conducting root cause analysis on assigned shifts/lines/areas and defining & assigning appropriate corrective actions.
Monitors, manages and reports on safety metrics for assigned shifts/lines/areas of responsibility on daily/weekly/monthly/ quarterly basis or as appropriate.
Responsible for recording safety issues, completing necessary safety paperwork, resolving the safety issue in a timely manner.
Supervisory
Accountable for managing the performance of all assigned personnel.
Documenting and delivering performance management for assigned staff including development and delivery of performance appraisals, performance feedback, employee development discussions, performance improvement plans and disciplinary decisions including introductory employment period.
Responsible for hiring suitably skilled and competent staff for assigned shifts/lines/areas.
Responsible for ensuring assigned staff receive timely on-boarding and on-going training.
Monitors, manages and reports (where appropriate) on employee performance metrics for assigned shifts/lines/areas of responsibility.
Carries out supervisory responsibilities in accordance with the organization’s policies and applicable laws.
QUALIFICATIONS
Bachelor's Degree, Operations Management, Engineering, or relevant course of study.
1 year - Related experience with supervisory skills in a manufacturing environment (Required)
5 years - Experience in a manufacturing environment, preferably medical devices (Required)
Knowledge and experience in Lean, Six Sigma, 5S (Required)