Quality Systems & Compliance Lead

Polygon Company; Indiana (PA); On-site; USD 80,000 - 100,000; Full time

Job summary

Polygon Company in Indiana, Pennsylvania, is seeking a Quality Systems & Compliance Lead. This key role involves ensuring the effectiveness of the Quality Management System (QMS) within a manufacturing setting and maintaining compliance with ISO standards.

The ideal candidate has over 7 years of experience in Quality Engineering, strong organizational skills, and the ability to influence cross-functionally. Key responsibilities include managing audits, driving quality improvements, and translating regulatory requirements into actionable processes.

Qualifications

• 7+ years of experience in Quality Systems, Quality Engineering, or Manufacturing Quality.
• Demonstrated experience in a manufacturing environment.
• Strong understanding of quality systems in production settings.

Responsibilities

• Own and maintain the Quality Management System (QMS).
• Ensure compliance with ISO 9001, ISO 13485, and ISO 14001.
• Lead internal and external audit activities.

Skills

Regulatory requirements translation

Root cause analysis

Project management

Communication skills

Attention to detail

Education

Bachelor’s degree in engineering, Quality, Manufacturing, or related field

ISO Lead Auditor, ASQ CQE, CQA certifications

Tools

1factory or similar electronic QMS systems

Job description

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:
• ISO 9001 (required)
• ISO 13485 (required)
• ISO 14001 (preferred)
• AS9100 or IATF 16949 (preferred)
• Experience developing or managing internal audit programs
• Experience leading external audits (ISO and/or customer audits)
• 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.