Senior Post Market Quality Specialist - Littleton - 3D Systems

Description

What We Are Looking For

We are seeking a highly organized and quality-driven Sr. Post-Market Surveillance Specialist to lead key quality system processes including complaint handling, CAPA management, field corrective actions, and post-market surveillance (PMS). This role is responsible for ensuring timely and thorough investigations, driving cross-functional root cause analysis, developing PMS plans and reports, managing customer communications, and maintaining documentation that meets global regulatory requirements. The ideal candidate will have experience in regulated industries such as medical devices or aerospace, possess strong problem-solving and technical writing skills, and take a proactive, continuous improvement approach. This is a visible and impactful role that strengthens our quality system, protects customers, and supports regulatory compliance globally.

Onsite

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

What's in it for You

• Competitive Pay: $76,000 - $90,000 per year. Our employees are the best part of our company. We want you to feel valued, appreciated, and included. Because of this, we make sure your hard work is recognized.
• Paid Leave (US ONLY): Enjoy time away from work with Company paid holidays and a flexible working schedule through our paid time off (PTO) policy.Yep, you read that correctly. We are a Company that values you and makes sure you take time for yourself.
• 401(k): Prepare for a secure retirement with our 401k plan, which includes an employer matching contribution.
• Comprehensive Health & Wellness Plans: We offer a comprehensive benefit package that includes medical, dental and vision coverage, company-paid short-term and long-term disability insurance, as well as company-paid basic life insurance that supports you during your career with us. We believe that taking care of our employees is essential, and these benefits reflect our commitment to your health, security, and peace of mind.
• Global Team: With our state-of-the-art corporate headquarters in Rock Hill, South Carolina, our global team has a presence across more than 15 countries worldwide. Experience a workplace comprised of talented individuals who are passionate about serving our customers and each other.
• Innovative Culture: Innovation is at the heart of what we do Since our founding in 1986 by Chuck Hull, the inventor of 3D printing, we have continuously pushed the boundaries of what is possible with additive manufacturing. When you join 3D, you will have the opportunity to work with cutting edge technology in an innovative and collaborative culture
• Talent Development: At 3D Systems, we invest in talent programs to support employees with opportunities to grow, contribute, develop, and thrive in their careers.
• Connection & Engagement Opportunities: We strive to cultivate an environment where our diverse global workforce can connect and thrive. Our Employee Resource Group program, Employee Recognition program, and 3D Gives Back program, are just a few examples of how you will be empowered to build connections, celebrate wins, and make a meaningful impact.

What You Will Do

• Own and oversee the entire CAPA process as CAPA Coordinator, including leading the CAPA Review Board, ensuring CAPAs comply with internal procedures, and verifying technical writing is clear, accurate, and audit ready.
• Meet regularly with CAPA owners to provide feedback, guide root cause analysis (RCA) using appropriate methodologies (e.g., 5 Whys, Fishbone), and track corrective and preventive action items to ensure timely closure.
• Own the full complaints handling process, from intake and investigation to closure, ensuring all activities are thoroughly documented, complete, and meet global regulatory requirements.
• Manage all customer communications related to complaints, including initial acknowledgment, follow-up inquiries, requests for additional information, and providing final investigation results.
• Collaborate cross-functionally with Quality, Regulatory Affairs, Product Development, Manufacturing, and Service teams to ensure appropriate investigation, escalation, and resolution of product issues.
• Submit Medical Device Reports (MDRs) and other required regulatory reports (e.g., EU vigilance reports, Health Canada reporting) in a timely and accurate manner.
• Coordinate and manage Field Safety Corrective Actions (FSCAs) and recall activities, including preparation of regulatory submissions and customer notifications, as needed.
• Develop, maintain, and execute Post-Market Surveillance (PMS) activities, including PMS plans, PMS reports, and related processes to ensure compliance with global regulatory requirements.
• Monitor complaint trends, conduct data analysis, and escalate issues as appropriate to drive continuous improvement and product safety initiatives.
• Serve as Subject Matter Expert (SME) for internal and external audits related to CAPA, complaints, and post-market surveillance processes.

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 in Quality, preferably with a focus on CAPA, complaints, or post-market surveillance required.
• Experience in FDA-regulated and/or ISO-certified environments required.

Required Skills/Abilities

• Strong attention to detail with technical documentation and writing skills
• Proven ability to conduct and document thorough investigations, root cause analyses, and CAPA processes.
• In depth knowledge of quality system regulations and standards (e.g., 21 CFR Part 820, ISO
• Ability to manage multiple priorities and meet deadlines in a fast-paced, regulated environment.
• Effective cross-functional communication, collaboration, and problem-solving skills.

Preferred Experience

• Knowledge of FDA 21 CFR Part 820, ISO 13485, and relevant quality system regulations.
• Experience with AS9100 or aerospace quality systems.
• Familiarity with Medical Device Reporting (MDR) and vigilance activities.
• Experience with Post-Market Surveillance (PMS) activities, including reports and trend analysis.
• Coordination of field corrective actions (FSCAs), recalls, and regulatory submissions.
• Experience in CAPA, complaint, and PMS processes and audits.
• ASQ certifications (e.g., CQA, CQE, CSQP) a plus.

Applications accepted online through February 13th, 2026

#LI-MM1

3D Systems is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to, among other things, race, color, ethnicity, religion, sex, age, sexual orientation, genetic information, marital status, gender identity or national origin or because he or she is an individual with a disability or a disable veteran, Armed Forces service medal veteran (referred to collectively as "protected veterans"). The Company also provides applicants with equal employment opportunities without regard to pregnancy, childbirth, medical needs arising from pregnancy or childbirth, and related medical conditions including, but not limited to, lactation. Primary Location: US-CO-Littleton Work Locations: USA-CO-Littleton 80127 Travel: No Type of Position: Employee Job Posting: Jan 29, 2026, 5:36:43 PM