Quality Systems & Compliance Lead at Polygon Company

Walkerton, Indiana, United States -

Full Time

Start Date

Immediate

Expiry Date

04 Sep, 26

Salary

0.0

Posted On

06 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Management System, ISO 9001, ISO 13485, ISO 14001, Internal Auditing, CAPA, Document Control, Root Cause Analysis, Compliance Management, Cross-functional Collaboration, Project Management, Manufacturing Quality, eQMS, Regulatory Compliance, Process Improvement, Audit Leadership

Industry

Manufacturing

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.

Responsibilities

The Lead is responsible for owning and maintaining the effectiveness of the Quality Management System (QMS) to ensure compliance with ISO standards. They bridge the gap between regulatory requirements and practical manufacturing processes while leading internal and external audit activities.