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Quality Supervisor

Omnicell

St Petersburg, FLOnsitePosted 16 days ago
Full TimeSenior LevelQuality (QA / QC)Medical Device
Original posting ↗

Summary

At Omnicell, quality is about more than meeting specifications. It's about building products people can depend on and delivering outcomes that matter. We're looking for a Quality Supervisor to join our Quality Operations team onsite in St. Petersburg, Florida. You'll lead frontline quality operations and partner closely with Operations, Manufacturing Engineering, Supply Chain, Supplier Quality, Customer Support, and Quality Engineering to ensure our products consistently meet customer, regulatory, and business requirements.

Job description

This is a hands-on leadership role for someone who enjoys solving complex problems, developing people, and turning data into action. You'll lead a talented quality team, strengthen incoming, in-process, and final inspection activities, drive root cause investigations, and champion improvements that enhance both quality and operational performance.

What You'll Do

  • Lead, coach, train, and develop Quality team members while assigning daily priorities and supporting strong team performance.
  • Provide guidance on incoming inspection requirements and lead related change management activities.
  • Manage nonconforming material processes, including investigations, evaluation, and disposition.
  • Lead root cause analysis and corrective action activities using methodologies such as fishbone analysis, 8D, CAPA, and design of experiments.
  • Define and improve inspection techniques and evaluate measurement equipment, emerging technologies, and AI-enabled inspection solutions.
  • Lead or participate in quality and continuous improvement projects that support departmental and business objectives.
  • Support the effectiveness and ongoing maintenance of the Quality Management System.
  • Serve as a change champion by identifying opportunities for improvement and helping teams successfully adopt new processes and ways of working.
  • Act as a key liaison between Quality and cross-functional partners across Omnicell.
  • Serve as a subject matter expert during internal and external audits.
  • Support quality activities associated with new products, manufacturing processes, and operational improvements.

What You'll Bring

  • Bachelor of Science degree.
  • 5+ years of supervisory experience in manufacturing quality, quality assurance, or quality control within a high-speed manufacturing environment.
  • Experience managing nonconforming materials, root cause investigations, corrective actions, and other quality investigations.
  • Demonstrated success leading continuous improvement initiatives using Lean, Six Sigma, or similar methodologies.
  • Working knowledge of quality management systems and standards such as ISO 9001.
  • Understanding of AQL levels within applicable ANSI standards.
  • Strong analytical, organizational, problem-solving, and decision-making skills.
  • Proficiency with Microsoft Office and experience with business or quality systems such as SAP, Smartsheet, or equivalent platforms.
  • Strong written and verbal communication skills with the ability to collaborate across functions and levels of the organization.
  • Ability to manage multiple priorities and detail-oriented projects in a fast-paced environment.

What Will Help You Stand Out

  • ASQ certification such as Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or Certified Manager of Quality/Organizational Excellence (CMQ/OE).
  • Experience supporting internal or external audits, supplier quality, validation and qualification activities, or statistical analysis.
  • Strong project management and organizational skills.
  • Ability to balance urgency with diplomacy, empathy, and sound judgment.
  • Strong attention to detail and the ability to deliver under tight deadlines.

Requirements

  • Bachelor of Science degree
  • 5+ years of supervisory experience in manufacturing quality, quality assurance, or quality control within a high-speed manufacturing environment
  • Experience managing nonconforming materials, root cause investigations, corrective actions, and other quality investigations
  • Demonstrated success leading continuous improvement initiatives using Lean, Six Sigma, or similar methodologies
  • Working knowledge of quality management systems and standards such as ISO 9001
  • Understanding of AQL levels within applicable ANSI standards
  • Strong analytical, organizational, problem-solving, and decision-making skills
  • Proficiency with Microsoft Office and experience with business or quality systems such as SAP, Smartsheet, or equivalent platforms
  • Strong written and verbal communication skills with the ability to collaborate across functions and levels of the organization
  • Ability to manage multiple priorities and detail-oriented projects in a fast-paced environment

Company overview

Omnicell is a leading provider of medication management solutions and adherence tools for healthcare systems. Founded in 1992 and headquartered in Mountain View, California, the company specializes in developing automated systems for medication dispensing, inventory management, and pharmacy workflow optimization. Omnicell's comprehensive portfolio includes automated dispensing cabinets, central pharmacy automation systems, medication adherence packaging, and analytics software that help healthcare providers improve patient safety, operational efficiency, and medication adherence. The company serves hospitals, health systems, retail pharmacies, and long-term care facilities across the United States and internationally. Omnicell's technology solutions are designed to reduce medication errors, optimize inventory control, and streamline pharmacy operations through intelligent automation and data-driven insights. The company has established itself as a key player in healthcare technology, focusing on transforming medication management through innovative automation and digital solutions that enhance patient care quality while reducing healthcare costs.

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