Quality Control Supervisor at Champion Healthcare Solutions

Ocala, Florida, United States -

Full Time

Start Date

Immediate

Expiry Date

04 Jun, 26

Salary

0.0

Posted On

06 Mar, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Supervision, Quality Control, Inspection, ISO 13485:2016, cGMP, QSR 820, Recordkeeping, Compliance, Defect Investigation, Corrective Actions, Team Management, Coaching, Blueprint Interpretation, Technical Drawing Interpretation, Measurement Tools, Excel Proficiency

Industry

Hospitals and Health Care

Description

Description From the very beginning, Champion has been 100% focused on medical seating. We pride ourselves in being at the forefront of the industry to provide our customers with innovative, clinically effective solutions that improve performance for both patients and caregivers. We continue to set the standard for medical seating, and partner with healthcare organizations to support the industry’s transformation into an all-inclusive, human-centric experience. Quality Supervisor The Quality Control (QC) Supervisor is responsible for overseeing the daily activities of the quality inspection team, ensuring adherence to established inspection standards and regulatory requirements. This role supports production by maintaining quality oversight, identifying trends in defects, and ensuring accurate documentation of quality control activities. The QC Supervisor will escalate broader quality concerns, systemic issues, or personnel matters to Quality Engineering and the Director of Regulatory Affairs & Quality Assurance (RA/QA) as appropriate. Quality Supervisor Responsibilities · Supervise Quality Control Procedures – Oversee a team responsible for inspecting incoming materials, in-process components, and finished products to ensure compliance with ISO 13485:2016 quality control standards. · Work Assignment & Planning – Assign and manage daily tasks for the QC team to ensure coverage and efficiency in inspection activities, and in alignment with goals set by the department. · Issue Identification & Escalation – Keep the Director of RA/QA and Quality Assurance team informed of any issues affecting personnel, inspection results, or production quality concerns. · Inspection Process Oversight – Ensure consistency and effectiveness in inspection procedures, collaborating with production teams to maintain quality standards. · Recordkeeping & Compliance – Maintain accurate inspection reports and quality records to ensure compliance with regulatory requirements. · Defect Investigation & Resolution – Assist in identifying and containing defective products, documenting findings, and working with production to implement corrective actions. · Team Management & Morale – Provide guidance, coaching, and support to QC inspectors. · Training & Process Adherence – Support ongoing training of QC personnel on inspection techniques, documentation, and work instructions to ensure consistent application of quality control procedures. Requirements Qualification Requirements: · Knowledge of cGMP, QSR 820, ISO 13485, and basic quality control principles. · Strong organizational and communication skills to manage team coordination and reporting. · Ability to interpret and apply quality standards, work instructions, and product specifications. · Experience collaborating with production teams to maintain quality requirements. · Blueprint & Technical Drawing Interpretation Competencies: · Technical capacity – blueprint/technical drawing interpretation, proficiency using measurement & inspection tools, tolerance analysis · Microsoft Excel proficiency (data entry, basic analysis, tracking quality trends) · System support & data management (ERP/QMS experience preferred) · Communication · Follow through · Detail Oriented. · Teamwork · Results Driven Education and/or Experience: · Associate’s degree in a related field preferred. · 4-6 years of experience in a Medical Device Manufacturing environment with hands-on QC experience (any level).

Responsibilities

The Quality Control Supervisor oversees the daily activities of the inspection team, ensuring adherence to established standards for incoming materials, in-process components, and finished products according to ISO 13485:2016. This role involves assigning tasks, identifying quality trends, maintaining accurate records, and escalating systemic issues to Quality Engineering and the Director of RA/QA.