Description GENERAL The Quality Systems & Compliance Lead is responsible for owning and maintaining the effectiveness of Polygon's Quality Management System (QMS) within a hands-on manufacturing ...
Description GENERAL The Quality Systems & Compliance Lead is responsible for owning and maintaining the effectiveness of Polygon's Quality Management System (QMS) within a hands-on manufacturing ...
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Be Seen First
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$21 - $23/hr
Develop expertise regarding Trifecta Medical's QMS to be a consistent resource to Operations personnel, peers, etc. * Ensure proper documentation, quality records, etc. * Assist in any/all other ...
GENERAL The Quality Systems & Compliance Lead is responsible for owning and maintaining the effectiveness of Polygon's Quality Management System (QMS) within a hands-on manufacturing environment.
Quick apply
GENERAL The Quality Systems & Compliance Lead is responsible for owning and maintaining the effectiveness of Polygon's Quality Management System (QMS) within a hands-on manufacturing environment.
You will be a key player in maintaining our Quality Management Systems (QMS) and inventory databases while providing essential help-desk support to our team. In addition, you will assist with ...
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Qms information
See Indiana salary details
$33.7K - $46.3K
2% of jobs
$46.3K - $59K
7% of jobs
$59K - $71.7K
11% of jobs
$77.7K is the 25th percentile. Wages below this are outliers.
$71.7K - $84.4K
11% of jobs
$84.4K - $97.1K
11% of jobs
$97.1K - $109.7K
7% of jobs
The median wage is $114.5K / yr.
$109.7K - $122.4K
4% of jobs
$132.4K is the 75th percentile. Wages above this are outliers.
$122.4K - $135.1K
28% of jobs
$135.1K - $147.8K
1% of jobs
$147.8K - $160.4K
1% of jobs
$160.4K - $173.1K
17% of jobs
$33.7K
$114.1K
$173.1K
How much do qms jobs pay per year?
What is the difference between Qms vs Quality Assurance Specialist?
| Aspect | Qms | Quality Assurance Specialist |
|---|---|---|
| Certifications | ISO 9001 Lead Auditor, Quality Management certifications | ISO 9001, Six Sigma, CQE |
| Work Environment | Manufacturing, industrial, or service sectors focusing on quality systems | Manufacturing, software, healthcare, and various industries |
| Employer & Industry Usage | Organizations implementing quality management systems | Companies ensuring product/service quality |
| Search & Comparison Intent | Understanding quality system implementation | Quality process evaluation and improvement |
Qms professionals focus on establishing, maintaining, and auditing quality management systems within organizations, often working with standards like ISO 9001. Quality Assurance Specialists concentrate on testing, inspection, and ensuring products or services meet quality standards. While both roles aim to improve quality, Qms roles are more system-oriented, whereas Quality Assurance Specialists are more product-focused.
What skills and qualifications are needed to thrive as a QMS professional?
What is the job description of a QMS?
What are common challenges faced by QMS professionals, and how can they be managed?
What does a QMS professional do?
What is a QMS job?

Full-time
Re-posted 3 days ago
Job description
Description
GENERAL JOB DESCRIPTION
The Quality Systems & Compliance Lead is responsible for owning and maintaining the effectiveness of Polygon's Quality Management System (QMS) within a hands-on manufacturing environment. This role ensures compliance to ISO 9001, ISO 13485, and ISO 14001 while driving practical application of quality system requirements across both Medical and Industrial operations.
This position bridges compliance and manufacturing by translating regulatory requirements into effective, usable processes on the production floor. The role leads internal and external audit activities, drives system-level improvements, and ensures consistency across the organization.
This is a senior individual contributor role with significant cross-functional influence
Requirements
DUTIES & RESPONSIBILITIES
Own and maintain the company's Quality Management System (QMS) within the electronic QMS platform (1factory)
Ensure compliance with ISO 9001, ISO 13485, and ISO 14001 requirements
Develop, implement, and maintain the internal audit program
Conduct internal audits and ensure timely closure and effectiveness of findings
Serve as primary lead for ISO certification audits and support customer audits
Translate ISO and regulatory requirements into practical, executable manufacturing processes
Identify gaps in processes and drive system-level improvements
Own and maintain the CAPA process, ensuring structured root cause analysis and effective corrective actions
Monitor CAPA performance, including closure timelines and effectiveness verification
Own document control system governance, including workflows, revision control, and training alignment
Execute or directly support document control activities as needed, including document release, revision, and workflow management within the eQMS.
Ensure training is assigned, tracked, and completed in alignment with document changes prior to implementation.
Partner with Operations and Engineering to ensure quality processes are aligned with real manufacturing practices
Provide guidance and support to cross-functional teams on document creation, formatting, and compliance expectations.
Support Quality Engineers and Supervisors with system-related guidance and best practices
Standardize quality system processes across Medical and Industrial divisions
Ensure audit readiness across all departments and functions
EDUCATION & TRAINING
Bachelor's degree in engineering, Quality, Manufacturing, or related field preferred
Relevant certifications (e.g., ISO Lead Auditor, ASQ CQE, CQA) preferred
KNOWLEDGE & EXPERIENCE
7+ years of experience in Quality Systems, Quality Engineering, or Manufacturing Quality
Demonstrated experience in a manufacturing environment (high-mix preferred)
Strong understanding of how quality systems are applied in production settings
Experience working with one or more of the following standards:
o ISO 9001 (required)
o ISO 13485 (required)
o ISO 14001 (preferred)
o AS9100 or IATF 16949 (preferred)
Experience developing or managing internal audit programs
Experience leading external audits (ISO and/or customer audits)
o Experience with electronic QMS systems (1factory or similar preferred)
SKILLS & ABILITIES
Strong ability to translate regulatory requirements into practical manufacturing processes
Effective root cause analysis and problem-solving skills
Strong organizational and project management skills
Ability to work independently and drive initiatives without direct supervision
Excellent communication and cross-functional collaboration skills
Ability to influence without direct authority
Strong attention to detail with a systems-level mindset
WORKING CONDITIONS
The physical demands are representative of those that must be met by an associate to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, associate is regularly required to sit, stand, stoop, climb, walk, use hands, talk, and hear for a minimum of eight (8) hours per shift
HOURS / SHIFTS
Varies depending on project and customer needs.
About Polygon.io
Sourced by ZipRecruiter
Industry
Finance and insurance
Company size
11 - 50 Employees
Headquarters location
Atlanta, GA, US
Year founded
2016