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Qms Jobs in Indiana (NOW HIRING)

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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 ...

Quality Engineer

Indianapolis, IN · On-site

$75K - $85K/yr

Manage controlled changes within the QMS in collaboration with the Quality Manager and relevant departments. The ideal candidate: Strong understanding of quality management systems (e.g., ISO 9001 ...

Quality Engineer

Noblesville, IN · On-site

$67K - $87K/yr

The objective of this position is to provide the level of resource necessary to maintain, monitor and improve the Quality Management System (QMS) for Ambu USNV, to ensure compliance with regulatory ...

The right candidate will help drive the adoption and improvement of strategic QMS processes that will shape the QMS culture of our facility. Maintaining compliance with applicable customer and ...

Showing results 21-40

Qms information

See Indiana salary details

$33.7K

$114.1K

$173.1K

How much do qms jobs pay per year?

As of Aug 8, 2026, the average yearly pay for qms in Indiana is $114,103.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,400.00 and $150,500.00 per year, depending on experience, location, and employer.

What is the difference between Qms vs Quality Assurance Specialist?

AspectQmsQuality Assurance Specialist
CertificationsISO 9001 Lead Auditor, Quality Management certificationsISO 9001, Six Sigma, CQE
Work EnvironmentManufacturing, industrial, or service sectors focusing on quality systemsManufacturing, software, healthcare, and various industries
Employer & Industry UsageOrganizations implementing quality management systemsCompanies ensuring product/service quality
Search & Comparison IntentUnderstanding quality system implementationQuality 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?

To thrive as a Quality Management System (QMS) Specialist, you need a solid understanding of quality standards (such as ISO 9001), process improvement methodologies, and experience with audits, often supported by a degree in engineering or a related field. Familiarity with QMS software platforms, document control systems, and relevant certifications like ISO 9001 Lead Auditor or Six Sigma is typically required. Strong attention to detail, analytical thinking, and effective communication are vital soft skills for ensuring compliance and driving quality initiatives. These skills and qualifications are important because they help organizations maintain regulatory compliance, improve efficiency, and deliver high-quality products or services.

What is the job description of a QMS?

A Quality Management System (QMS) professional is responsible for developing, implementing, and maintaining quality standards and procedures within an organization. They conduct audits, analyze data, and ensure compliance with industry regulations to improve product or service quality. Familiarity with quality tools like ISO standards and proficiency in documentation and process improvement are essential skills for this role.

What are common challenges faced by QMS professionals, and how can they be managed?

Professionals in QMS roles often encounter challenges such as ensuring consistent compliance with changing industry regulations, promoting a culture of quality across diverse teams, and managing documentation efficiently. Effective communication and regular training are vital for keeping teams aligned with quality standards. Additionally, implementing robust digital tools for document control and ongoing audits can streamline processes and make regulatory compliance more manageable. Collaboration with cross-functional teams is key to identifying improvement opportunities and resolving quality issues promptly.

What does a QMS professional do?

QMS professionals are experts who manage and implement Quality Management Systems within organizations. Their main role is to ensure that a company’s products or services consistently meet customer and regulatory requirements by developing, maintaining, and improving quality policies and procedures. They conduct audits, facilitate compliance with standards like ISO 9001, and drive continuous improvement initiatives. QMS professionals work across industries such as manufacturing, healthcare, and services to help organizations achieve high standards of quality and efficiency.

What is a QMS job?

A QMS (Quality Management System) job involves developing, implementing, and maintaining quality standards within an organization to ensure products or services meet specified requirements. It often requires knowledge of quality standards like ISO 9001, auditing skills, and attention to detail. QMS professionals work to improve processes, ensure compliance, and support continuous quality improvement.
What are the most commonly searched types of Qms jobs in Indiana? The most popular types of Qms jobs in Indiana are:
What are popular job titles related to Qms jobs in Indiana? For Qms jobs in Indiana, the most frequently searched job titles are:
What cities in Indiana are hiring for Qms jobs? Cities in Indiana with the most Qms job openings:
Infographic showing various Qms job openings in Indiana as of August 2026, with employment types broken down into 91% Full Time, 3% Part Time, 5% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $114,103 per year, or $54.9 per hour.

Quality Systems & Compliance Lead

Polygon Company

Walkerton, IN • On-site

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.