Floor Supervisor

Angel Aligner; Oak Creek (WI); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Competitive base salary and benefits

Job summary

Angel Aligner is seeking a Floor Supervisor to oversee daily production on the manufacturing floor, ensuring safety, quality, and productivity targets are met in compliance with FDA, GMP, ISO 13485, and internal quality systems. The role leads operators, coordinates workflow, resolves issues, and ensures documentation meets regulatory standards.

You will monitor output, cycle times, scrap, and efficiency; enforce SOPs; support start‑up, changeover, and shutdowns; train team members; and partner

Qualifications

• 3+ years of manufacturing experience, preferably in regulated industries.
• 1+ year of leadership or lead-operator experience.
• Strong knowledge of GMP, ISO 13485, and FDA-regulated production.
• Ability to read and interpret work instructions and basic technical drawings.

Responsibilities

• Assigns work and balances labor to meet schedule demands.
• Monitors production output, cycle times, scrap, and efficiency metrics.
• Ensures adherence to SOPs, work instructions, and validated processes.
• Supports start-up, changeover, and shutdown activities.
• Enforces GMP, GDP, and cleanroom/controlled-environment requirements.
• Ensures documentation like Device History Records (DHRs) is accurate.
• Escalates and documents nonconformances; supports investigations.
• Partners with Quality to address inspection failures and process issues.
• Ensures operators follow inspection, handling, and traceability procedures.
• Provides training and development to team members; reduces turnover.
• Drives safety, accountability, and continuous improvement culture.
• Addresses attendance, behavior, and performance promptly.
• Maintains audit-ready production areas; conducts safety checks.

Skills

Leadership

Communication

Problem solving

Reading drawings

Tools

ERP/MES systems

Job description

Job Summary: The Floor Supervisor oversees daily production activities on the manufacturing floor to ensure safety, quality, and productivity targets are met in compliance with FDA, ISO 13485, and internal quality‑system requirements. This role leads operators, coordinates workflow, resolves production issues, and ensures that all documentation and processes meet regulatory standards.

Essential Functions:

• Assigns work, balances labor, and adjusts staffing to meet schedule demands.
• Monitors production output, cycle times, scrap, and efficiency metrics.
• Ensures adherence to work instructions, SOPs, and validated processes.
• Supports start‑up, changeover, and shutdown activities.
• Enforces GMP, GDP, and cleanroom/controlled‑environment requirements.
• Ensures accurate completion of Device History Records (DHRs) and production documentation.
• Escalates and documents nonconformances; supports NCR investigations.
• Partners with Quality to address inspection failures, deviations, and process issues.
• Ensures operators follow proper inspection, handling, and traceability procedures.
• Be responsible for team member training and competency development, implementing initiatives to reduce employee turnover.
• Conducts performance feedback and support skill development.
• Promotes a culture of accountability, safety, and continuous improvement.
• Addresses attendance, behavior, and performance issues promptly.
• Enforces safety policies and ensure proper use of PPE.
• Conducts safety checks and support incident investigations.
• Maintains a clean, organized, and audit‑ready production area.
• Identifies bottlenecks, waste, and processes inefficiencies.
• Supports Lean, 6S, and Kaizen initiatives.
• Provides feedback to engineering on equipment, tooling, and processes improvements.
• Collaborate with Engineering, Quality, Supply Chain, and Warehouse to support NPI, process optimization, and material supply.
• Report production KPIs including output, efficiency, yield, cost, and quality.
• Ensure EHS compliance; eliminate safety risks and maintain a safe working environment.

Qualifications:

• 3+ years of experience in manufacturing, ideally medical device, pharma, aerospace, or other regulated industries.
• 1+ year of leadership or lead‑operator experience.
• Strong understanding of GMP, ISO 13485, and FDA‑regulated production.
• Ability to read and interpret work instructions, SOPs, and basic technical drawings.
• Excellent communication, problem‑solving, and decision‑making skills.
• Ability to work on-site in a manufacturing environment.

Preferred but not required Qualifications:

• Experience supervising cleanroom operations.
• Familiarity with ERP/MES systems (SAP, Oracle, etc.).
• Knowledge of Lean Manufacturing tools (5S, root‑cause analysis, standard work).
• Experience supporting audits or regulatory inspections.
• Strong problem‑solving and critical‑thinking skills
• High attention to detail and documentation accuracy
• Ability to work cross‑functionally in a fast‑paced environment
• Commitment to patient safety and product quality

Physical and Work Environment Requirements:

• Ability to stand for extended periods.
• Manual dexterity for handling small components.
• Work in cleanroom or controlled‑environment areas as required.
• Occasional travel for supplier audits or training
• Ability to lift up to 40 lbs
• Travel is approximately 5% with international overnight stays required
• We offer a competitive base salary and benefits.