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in Fort Lauderdale, FL
Production Group Leader
•30 days ago
Hours | Full-time, Part-time |
---|---|
Location | Fort Lauderdale, FL Fort Lauderdale, Florida |
About this job
JOB DESCRIPTION:
- Support and complies with PL Developments’ Quality System, ISO, FDA, cGMP, and local regulations within the medical device requirements
- Assign tasks to Set-Up Technicians, Material Handlers, and Production Employees
- Execute against daily production schedule and assist operators in daily manufacturing tasks and projects
- Provide a safe work environment and ensures adherence to all safety policies
- Communicate and enforces all safety processes and procedures
- Investigate and reports all safety related incidents
- Provide training and coaching to full time and temporary employees
- Ensure compliance with quality specifications and oversee the in-line process of quality control
- Follow procedures described in SOP’s and report deviations to Manufacturing Manager
- Practice/Enforce Good Manufacturing procedure as trained in cGMP training
- Facilitate and cooperate with any Continuous Improvement Program
- Write process deviations, non-conformance reports, SOP, WI, CAPA and investigations
- Schedule monthly, weekly and daily activities based on planning reports
- Manage team performance and provides solutions
- Enforce general housekeeping and operation’s integrity
- Report daily activities and produce required reports
- Ensure proper execution of all procedures in the production floor
- Audit performance, ensuring quality and compliance of the manufactured product
- Identify and report incapable processes: recipe, equipment, and documentation
- Understand and meets assigned metrics and key process indicators
- Manage team performance and provides solutions
- Support, drives, and improves workplace organization (5S)
- Enable effective communication between management and operators
- Read and complies with work instructions and batch records, and checklists
- Accurately records and reports hours worked
- Complete all other work duties as assigned
- High School diploma or equivalent
- 5-7 years manufacturing experience
- Experience in a medical device manufacturing environment
- Strong communication skills
- Demonstrated proficiency in the English Language, both written and oral
- Basic knowledge of Microsoft Word and Excel
- Basic knowledge of math for manufacturing
- Highly organized and attention to detail
- Strong problem-solving skills
- Ability to prioritize work and manage multiple tasks
- Ability to multitask and meet changing deadlines
- Adhere to pre-established manufacturing schedule
- Must be self-directed and able to complete projects with limited supervision.
- Ability to take direction from the production manager
- Ability to collaborate and assist team managers, peers and subordinates