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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