Job Details

ID #51706837
Estado Colorado
Ciudad Littleton
Full-time
Salario USD TBD TBD
Fuente 3D Systems, Inc.
Showed 2024-05-15
Fecha 2024-05-16
Fecha tope 2024-07-15
Categoría Etcétera
Crear un currículum vítae
Aplica ya

Development Quality Engineer II

Colorado, Littleton, 80120 Littleton USA
Aplica ya

Job Title: Development Quality Engineer II Company Overview: 3D Systems Healthcare Solutions is a leading player in the medical device industry, dedicated to improving healthcare through innovation and cutting-edge technology. We are seeking a qualified Intermediate Quality Engineer to join our New Product Development (NPD) team to ensure the quality and safety of our products. Job Description: Overview: As an Intermediate Product Development Quality Engineer, you will play a pivotal role in the design, development, and quality assurance processes of cutting-edge medical devices. You will work closely with cross-functional teams to ensure compliance with industry regulations, meet customer expectations, and deliver high-quality products to the market. Responsibilities: · Collaborate closely with cross-functional product development teams to establish, implement, and maintain quality standards throughout the product development life cycle. · Develop, execute, and oversee risk management activities, including risk assessments, hazard analyses, and risk mitigation strategies, in compliance with industry regulations and standards. · Provide input and review and approve product and process validation activities. · Lead and participate in design and process failure mode and effects analysis (DFMEA and PFMEA). · Identify and development of test methods, inspection plans, and quality control procedures. · Ensure compliance with applicable regulatory requirements, such as FDA, ISO, ITAR, and other relevant standards. · Investigate and address product non-conformances, root cause analysis, and implement corrective and preventive actions (CAPA) where appropriate. · Provide guidance and support to the design and engineering teams to address quality concerns and improve product design and manufacturability. · Assist in supplier quality management and supplier audits to ensure the quality of incoming materials and components. · Maintain accurate quality documentation, including design history files, risk management files, and test records. · Collaborate with regulatory affairs and provide input for regulatory submissions. · Continuously monitor industry trends and regulatory updates to stay current with best practices and compliance. Qualifications: · Bachelor's degree in engineering, preferably in biomedical, mechanical, or a related field; or equivalent combination of education and experience. · 3-5 years of experience in quality engineering, preferably in the medical device industry. · Knowledge of medical device regulations and standards (e.g., FDA 21 CFR Part 820, ISO 13485, ISO 14971). · As this role includes development of parts covered under ITAR, candidate must be a US Person. · Strong understanding of quality tools and methodologies, including FMEA, CAPA, and statistical analysis. · Quality certifications (e.g., ASQ Certified Quality Engineer) desirable. · Experience with product and process validation, design control, and risk management. · Excellent problem-solving and analytical skills. · Strong communication and interpersonal skills to collaborate effectively with cross-functional teams. · Detail-oriented with a high level of accuracy in documentation. · Ability to work independently and prioritize tasks in a fast-paced environment. · Applied experience with and understanding of additive manufacturing a plus. Benefits: · Competitive salary and benefits package. · Opportunities for professional growth and development. · A collaborative and innovative work environment. · Access to cutting-edge technology and resources. · Contribution to the development of life-saving medical devices. The Good Stuff! · Salary Range: $75,000 - $100,000 (Salary to be determined by the education, experience, knowledge, skills, and abilities of the candidate, and alignment with market data) · In addition to a salary, this position is eligible for an annual bonus based upon company performance. · 3D Systems offers a comprehensive benefit package including medical, dental and vision coverage, company-paid short-term and long-term disability insurance, and company-paid basic life insurance. Sick Leave, Flex (Vacation) Time, Parental Leave, and 8 holidays per year are also provided as paid time off. 3D Systems also provides a 401(k) Retirement Savings Plan option with a company match. Applications accepted online through May 21, 2024. Title: Development Quality Engineer II Location: CO-Littleton Requisition ID: 2400007I

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