Veranex

Quality Engineer 2

Veranex  •  $67k - $95k/yr  •  Providence, RI (Onsite)  •  1 month ago
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Job Description

Veranex’s mission as an Innovation CRO is to improve patient outcomes by accelerating our clients’ innovations to market. As the world’s only end-to-end professional services firm focused on MedTech, we take clients’ Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.

About This Role
Veranex has an exciting opportunity to join our team as a Quality Engineer 2. You will be part of a team working to improve lives globally through medical technology innovation. The Quality Engineer organizes and coordinates the quality activities for clients to help identify and meet quality engineering and quality management system (QMS) needs. Evaluates design inputs, outputs and design changes for quality requirements, risk management and impact assessment. Collaborate with clients to assure quality, risk, or other management plans for design, production and maintenance processes for general and specific product performance needs are established according to the client’s AMS while ensuring these activities are in accordance with industry standards and regulations. Focus is product lifecycle; design control, design transfer, production, and change management and processes for general and specific product performance needs.

What You Will Do
• Leads the administration of device design and change management and performs quality engineering activities with clients to assure quality controls and design changes meet requirements
• Conducts process risk management for novel and existing medical devices (PFMEA)
• Develops, documents, and validates inspection and test methods to support design control Process Validation, in-process inspection, and final inspection activities.
• Provides input and/or oversight for quality system related activities, including complaint handling, CAPA investigation and supplier evaluations, as needed to assist clients in ensuring product quality and proper implementation of compliant processes.
• Participates in continuous improvement efforts related to quality engineering processes
• Participates in continuous improvement efforts related to quality engineering processes.
• May support business development by participating in potential client meetings, educating clients, and providing proposal input.

Required Qualifications
• Bachelor’s degree in engineering or life sciences, or an equivalent combination of education, training, and experience
• 2-4 years of relevant experience in medical devices
• Experience mentoring/training other engineers
• Strong knowledge of medical device regulations, guidance documents and standards (i.e., quality system regulations (QSR) International Organization for Standardization (ISO) 13485, ISO 14971, ISO 62304, related ASTM, ANSI, AAMI, TIR standards and guidance documents as needed)
• Strong understanding of full product life cycle, including definition of customer needs, development, design testing, design transfer, manufacturing scale up, distribution, service, and post market analysis
• Strong understanding of concepts and principles of Quality Assurance with respect to new product development, regulatory bodies, external suppliers, product manufacturing and product servicing
• Excellent written and verbal communication skills
• Excellent attention to detail

Preferred Qualifications
• Demonstrated experience with client management
• Experience with different quality management systems
• Provides risk management expertise in the evaluation and design of product, design validation and verification

Location
• This is an onsite position in Providence, RI

Veranex is an equal opportunity employer and prohibits discrimination of any kind. All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.
Veranex

About Veranex

Veranex is the world's first global Innovation Contract Research Organization (iCRO) providing integrated product development and contract research services for medical device and in-vitro diagnostic companies.

Founded in 2021 but with a legacy over 20 years, Veranex combines design engineering, preclinical research, clinical trials, regulatory affairs, quality consulting, manufacturing, and market access services under one roof. This integrated approach eliminates traditional handoffs between development phases, reducing timelines and budget variance for clients.

The company serves medical device innovators from early-stage startups to global strategics across cardiovascular, neurovascular, ophthalmology, and diagnostic markets. With more than 800 specialists across North America, Europe, and Asia-Pacific, Veranex has supported over 1,000 device programs and 2,500 clinical trials (preclinical-feasibility and pivotal).

Headquartered in Raleigh, North Carolina, Veranex operates facilities in the US, Europe and Asia-Pacific with 15+ innovation and research centers.

For more information, visit https://veranex.com/

Industry
Biotech & Life Sciences
Company Size
501-1,000 employees
Headquarters
Raleigh, North Carolina
Year Founded
2021
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