Director, Quality
Company: Morgan Stanley
Location: Littleton
Posted on: June 1, 2025
Job Description:
The Quality Director will develop and enhance 3D Systems'
comprehensive healthcare quality strategy while ensuring customer
satisfaction and corporate goals are consistently achieved or
exceeded. This role also serves the needs of industrial
manufacturing and requires dynamic collaboration across Advanced
Manufacturing, Personalized Health Services, Medical Devices, and
the Application Innovation Group. The role partners Quality
leaders, Manufacturing Engineering, Production staff for healthcare
and industrial products, and our Regulatory team to promote and
deliver clear alignment across the organization. You'll define an
innovative quality roadmap that simultaneously improves customer
satisfaction, employee engagement, and stakeholder value while
serving as a transformational change agent. Join us in shaping the
future of manufacturing and making a meaningful impact on additive
manufacturing innovation at one of the industry's most
forward-thinking companies!OnsiteThis role has an onsite work
schedule requiring the person to be in the onsite location
(Littleton, CO) 5 days a week.What's in it for You!
- Competitive Pay: $162,000 - $200,000 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 DoOversee Quality Teams at
in US and Belgium:
- Lead and mentor Quality Teams across Littleton (CO), and Leuven
(Belgium)
- Provide clear strategy and vision aligned with business
objectives.
- Manage staffing, performance evaluations, and career
development.
- Set employee objectives linked to business initiatives and key
performance indicators.
- Direct quality management systems activities across all
sites.
- Oversee Management Review processes, Customer Complaint
Systems, and CAPA Systems for healthcare.
- Manage Training programs, Supplier Quality, and Internal Audit
Systems.
- Ensure regulatory compliance.
- FDA Quality System Regulation (21 CFR Part 820) registration
and inspection readiness.o Maintain ISO 13485, ISO 9001, MDSAP
(Medical Device Single Audit Program), Medical Device Regulation
(MDR), AS/EN 9100 certifications.o Other applicable ISO/EN
standards based on product portfolio and regional requirements
- Support Design Control procedures for all New Product
Introduction (NPI) initiatives.
- Lead the implementation and maintenance of a robust Risk
Management process in accordance with ISO 14971, ensuring
integration across the product lifecycle and alignment with global
regulatory expectations.
- Foster high-performing teams by embracing 3D Systems' corporate
values and employee engagement tools.Lead Strategic Quality
Initiatives:
- Develop and execute comprehensive quality strategy through
short term and long-term business planning.
- Serve as subject matter expert for critical quality functions,
specifically within the healthcare product lines.
- Lead product complaint investigations and CAPA root cause
analysis.
- Oversee nonconforming materials processes and
dispositions.
- Act as primary liaison for external compliance activities.
- Coordinate ISO, Regulatory, and Customer audits of Quality
Management Systems.
- Support internal and external audit activities.
- Lead QMS harmonization between Leuven and Littleton and eQMS
implementation across multiple sites.Partner with Cross-Functional
Teams:
- Collaborate with Engineering, Manufacturing, and R&D to
ensure integrated quality approach.
- Maintain compliance through strong design control and project
management understanding.
- Ensure quality, compliance, customer satisfaction, and patient
safety standards.
- Drive operational excellence through shared
accountability.
- Deliver on Cost of Poor Quality (COPQ) reduction and scrap
minimization.
- Improve on-time delivery and drive continuous process
improvements.
- Support manufacturing and component investigations while
participating in designated engineering projects.QualificationsWhat
You Will BringEducation and Training
- Bachelor's degree, preferably in engineering or related field;
or equivalent combination of education and experience.Required
Experience
- 10 years or more of Quality Assurance experience in medical
devices
- 5-7 years of quality assurance management experience
required
- Proven track record managing teams of individual
contributors
- Medical device and regulated industry expertise
- New Product Introduction (NPI) processes and lifecycle
management
- Verification and validation testing protocols
- High-reliability product development for medical or aerospace
industries
- Regulatory compliance experience
- FDA QSR, EU MDR, ISO 13485, and/or AS9100 expertiseKnowledge,
Skills & Abilities
- Advanced quality methodologies
- Total Quality Management (TQM) and Six Sigma programs
- Design of Experiments (DOEs) and statistical techniques
- Lean Thinking principles
- Leadership and management capabilities
- Ability to establish department goals and coordinate diverse
resources
- Strong task prioritization and problem-solving skills to ensure
timely completion
- Experience managing multiple projects simultaneously
- Communication and analytical skills
- Excellent verbal and written communication with internal and
external stakeholders
- Strong analytical, negotiation, and problem resolution
abilities
- Additional requirements
- This position serves the 3D Systems Quality Team and involves
work with export-controlled products for aerospace and defense
customers, requiring compliance with applicable export control
regulations.Preferred Experience
- Multi-site, multi-country operations experience
- Customer-facing experience in quality leadership roles
- CQE, CQA, CQM, ISO 13485:2016 Internal or Lead Auditor
Certifications preferred
- Certified Six Sigma Black Belt (CSSBB) - ASQ or equivalent
preferredApplications accepted online through June 9, 2025#LI-MP13D
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 LocationPrimary Location:
US-CO-LittletonWork LocationsWork Locations: USA-CO-Littleton
80127Job LevelJob Level: Manager with Direct ReportsTravelTravel:
Yes, 25 % of the TimeType of Position : EmployeeJob PostingJob
Posting: May 27, 2025, 3:00:02 PMAbout 3D Systems3D Systems
provides the most advanced and comprehensive 3D digital design and
fabrication solutions available today, including 3D printers, print
materials and cloud-sourced custom parts. Its powerful ecosystem
transforms entire industries by empowering professionals and
consumers everywhere to bring their ideas to life using its vast
material selection, including plastics, metals, ceramics and
edibles. Our leading personalized medicine capabilities save lives
and include end-to-end simulation, training and planning, and
printing of surgical instruments and devices for personalized
surgery and patient specific medical and dental devices. Its
democratized 3D digital design, fabrication and inspection products
provide seamless interoperabilityand incorporate the latest
immersive computing technologies. Our products and services disrupt
traditional methods, deliver improved results and empower its
customers to .manufacture the future now
#J-18808-Ljbffr
Keywords: Morgan Stanley, Greeley , Director, Quality, Executive , Littleton, Colorado
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