3D Systems Corporation

Senior Quality Systems Specialist

3D Systems Corporation • $75K — $95K *
Littleton, CO 80123In-Person
Aerospace & Defense
Less than 5 years of experience
Today
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Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering, Life Sciences, or a related field; or equivalent experience
  • 4-6 years of experience with Quality Management Systems in regulated industries
  • Strong knowledge of ISO 13485, FDA 21 CFR Part 820, MDSAP, EU MDR, and AS9100
  • Experience with internal audits and quality management activities
  • Proven collaboration and communication skills across various functions
  • Detail-oriented with the ability to prioritize tasks in a fast-paced environment

Responsibilities

  • Maintain and improve Quality Management System processes across sites
  • Monitor and implement updates to quality and regulatory requirements
  • Coordinate and administer the Internal Audit Program
  • Support audits from customers, certification bodies, and regulations
  • Coordinate responses to audit findings
  • Own and administer the CAPA program
  • Support supplier qualification and audit activities

Benefits

  • Onsite work schedule (5 days a week)
  • Opportunity to work in a high-visibility role
  • Engagement in continuous improvement initiatives
  • Exposure to various aspects of Quality Management and regulatory processes
  • Potential for professional growth and development in quality systems
Full Job Description
Description

What We Are Looking For

We are seeking a highly motivated Senior Quality Systems Specialist with a deep understanding of Quality Management Systems (QMS) in regulated industries such as medical devices or aerospace. The ideal candidate brings hands-on experience managing quality systems, strong cross-functional coordination skills, and a keen understanding of how quality processes drive both compliance and continuous improvement. This is a high-visibility role that requires a proactive communicator capable of managing complex quality deliverables while balancing regulatory rigor with business needs.

Onsite

This role has an onsite work schedule requiring the person to be in the onsite location 5 days a week.

What You Will Do

  • Maintain and improve Quality Management System processes across applicable sites and business functions.
  • Monitor changes to applicable quality and regulatory requirements and coordinate implementation of updates.
  • Coordinate and administer the Internal Audit Program, including scheduling, auditor assignments, audit tracking, and corrective action follow-up.
  • Support customer, certification body, and regulatory audits, including preparation, hosting activities, and follow-up actions.
  • Coordinate responses to audit findings resulting from customer, certification body, and regulatory audits.
  • Own and administer the CAPA program, including facilitation of investigations, effectiveness reviews, metrics, and closure activities.
  • Support supplier qualification and supplier audit activities as needed.
  • Support administration, validation, testing, and continuous improvement of the electronic QMS (eQMS).
  • Support document control and change management processes as required.
  • Prepare quality metrics, trend analysis, and Management Review inputs.
  • Participate in continuous improvement and risk-based quality initiatives.


Qualifications

What You Will Bring

Education and Experience

  • Bachelor's degree in a relevant discipline (e.g., Engineering, Life Sciences, or related field); or an equivalent combination of education and experience.
  • 4-6 years of experience working with Quality Management Systems in regulated industries (e.g., Medical Device, Aerospace, or Industrial Manufacturing)


Required Skills/Abilities

  • Strong working knowledge of relevant standards and regulations , including ISO 13485, FDA 21 CFR Part 820, MDSAP, EU MDR, and/or AS9100.
  • Familiarity with planning, conducting, participating or documenting internal audits.
  • Hands-on experience managing SCARs, CAPAs, or driving continuous improvement of QMS processes.
  • Comfortable using and maintaining a Quality Management System (QMS).
  • Excellent written and verbal communication skills, with a proven ability to collaborate effectively across functions and levels.
  • Strong attention to detail and ability to manage multiple priorities in a fast-paced environment.


Preferred Experience

  • Certified Lead Auditor (ISO 13485, ISO 9001, or AS9100).
  • Experience supporting third-party or regulatory audits (e.g., FDA, MDSAP, Notified Body).
  • Familiarity with training programs, document control, or change management.
  • Experience implementing or upgrading eQMS platforms.


Applications accepted online through October 9th, 2026

#LI-MP1

About 3D Systems Corporation

3D Systems Corporation is a leading provider of 3D printing solutions, including 3D printers, print materials, software, on-demand manufacturing services, and digital design tools. The company serves a wide range of industries, including aerospace, automotive, healthcare, dental, and consumer goods. 3D Systems was founded in 1986 and has since grown to become a global leader in the 3D printing industry, with operations in the Americas, Europe, and Asia. The company is committed to advancing the adoption of 3D printing technology and enabling its customers to create innovative products and solutions.
Learn more about 3D Systems Corporation
Size
1,721 employees
Market Cap
$941.6 million
Industry
Consumer Technology
Net Income
-$149.5 million
Founded
1986
5 Year Trend
-0.6%
Revenue
$557.2 million
NASDAQ
DDD
* Ladders Estimates

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