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Quality Manager

Job

QAI Laboratories Inc

Medley, FL (In Person)

Full-Time

Posted 8 weeks ago (Updated 7 weeks ago) • Actively hiring

Expires 5/27/2026

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Job Description

Quality Manager Medley, FL Job Details Full-time 1 day ago Benefits Health insurance Dental insurance Qualifications Quality control corrective actions EHS Accreditation standards (regulatory compliance area) Calibration Safety inspections for hazard identification Process optimization ISO standards Engineering Regulatory compliance Compliance audits & assessments Corrective and preventive actions (CAPA) Quality management Mid-level Compliance management implementation Key Performance Indicators Quality assurance audits Supervising experience Policy & process development Team management Performance Improvement (PI) Mentoring Organizational skills Developing new training programs Workplace health and safety regulatory compliance Quality audits Training & development 10 years
Full Job Description QAI Job Number:
QAI-CORP-QLTYMNGR-03112026 JOB TITLE
Quality Manager
LOCATION
Report to one of the QAI Locations (Rancho Cucamonga, CA; Tulsa, OK; Middleburg Heights, OH; Loves Park, IL; Medley, FL)
NUMBER OF POSITIONS
1
CATEGORY:
Quality, Safety, and Customer Experience
CLOSING DATE
Open until filled
BACKGROUND
QAI laboratories is a testing, calibration, inspection and certification organization providing services to manufacturers of Electrical Products, Building Products, Vehicles, Factory Built Structures and other regulated products. Recognition of the QAI name and logo have grown significantly over the past few years resulting in significant expansion of the business.
DUTIES:
The successful candidate will perform, but not limited to, the following responsibilities which will include: Assists in matters of QAI's quality system, accreditation, and safety regulatory compliance. Represent QAI during external audits from various accreditation bodies or partners companies. Work with employees to close Corrective Action Requests (CARs). Prepare and submit documentation to accreditors to close CARs. Track status of CARs from internal and external audits, complaints, etc. Ensure deadlines are met. Assist with accreditation scope expansion initiatives Schedule and perform internal audits of local areas of the QMS and assists the Director in performing internal audits throughout the organization. Identify areas of improvement in the local Quality System and recommend measures to carry out improvements. Write new policies, procedures, and lead implementation through training and education. Identify training needs in relation to the QMS and report these to senior management. Develop training plans for the QMS and implement the training as necessary. May prepare controlled documents for the QMS following QAI's processes. Revise controlled documents as directed by senior management May help to oversee the calibration program for different laboratory sites. May perform reviews of specific processes and implement improvement processes. Assist with the adoption of QAI QMS in locations Offer process improvement ideas and assist with carrying out process improvement and automation initiatives. The position may involve supervising or mentoring quality supervisors. Responsible for identifying risks and opportunities and working with the Director to plan and develop actions. Help develop Key Performance Indicators (KPIs) and track necessary data. Assist in the development of health and safety policies and procedures Help ensure Health and Safety policies are followed. Develop training as needed. Track completion of safety inspections at locations. May learn the technical requirements of various QAI business streams in order to provide added support. Other duties as may be required by the business from time to time.
QUALIFICATION
The successful candidate will have: Technical diploma in an Engineering discipline or equivalent and At least 10 years of relevant experience in conformity assessment or equivalent. Sound background in quality management and quality standards such as
ISO/IEC 17065, ISO/IEC 17025, ISO/IEC 17020, ISO
9001 or equivalent. Must be familiar with Microsoft M365 software Must have good written and oral skills.
Key Technical Competence:
Ability to read and comprehend accreditation standards and requirements. Ability to create, implement and maintain Quality Management System/Health Management System policies, procedures, and work instructions, to meet the requirements of
ISO 17025, ISO
17020, and ISO 17065 and other regulatory needs. Ability to identify best practices and able to implement and enforce these practices throughout the organization. Possesses adequate knowledge of the testing, inspection, and certification processes to audit these processes, and identify areas of improvement. Able to communicate ideas and innovations for improvements to the QAI QMS. Able to lead teams, work with diverse people, and implement process changes throughout the company.
APPLYING
QAI Laboratories offers a comprehensive compensation and benefits package including base salary and bonus/commissions, medical, dental, and other perks. We are committed to the long-term success of our employees. Interested? Please submit your resume and cover letter here. Check out our other career opportunities on our website careers page: qai.org/careers or reach out to the recruitment team at . Equal Opportunity Employer QAI Laboratories is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, marital status, political affiliation, sexual orientation, gender identity, genetic information, disability or protected veteran status. We are committed to providing a workplace free of any discrimination or harassment.
Note :
No sponsorship is available. •

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