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R&D Engineer - Charlotte, United States - Medical Murray
Description
Job DescriptionJob Description
The wage range for this position is $70,000 to $90,000. Compensation decisions are dependent on the specific details and circumstances of each candidate such as experience, skills, and education. Therefore, job title and salary range may vary.
Medical Murray
Title:
R&D Engineer
Location:
Charlotte, NC (*Onsite Position)
Some relocation assistance may be available
Due to continuous growth, we are searching for an experienced medical device
R&D Engineer .
Within the Medical Murray Engineering team, you will have a hands-on role in product development, designing and producing our clients' medical devices.
Our environment will offer a varied day with direct interaction with our clients in discussing assigned projects, next steps, and fielding our clients' questions.
Working collaboratively with the Medical Murray team in a high-energy environment, you will work on leading-edge technology as you roll out new medical devices to market.
Combining best-in-class design, development, and manufacturing expertise, Medical Murray's purpose is to help healthcare providers offer a higher quality of care, giving patients more time and a higher quality of life.
If you want to be part of a team like that, please applyAbout Medical Murray:
Since 1996, Medical Murray has been a privately owned company producing finished medical devices, components, and subassemblies for customers around the world ranging from startups to the largest OEMs.
We specialize in the development, testing, and manufacturing of permanent implants, delivery systems, and complex catheters for vascular, gastrointestinal, urologic, and other interventional markets.
Our core goals are Integrity First, People Matter, First Class Service, Inspired Innovation, and Community Service. To learn more, please visit us atPosition Summary:
Reporting to the R&D Engineering Manager, The R&D Engineer position performs the function of design engineer for product development work on medical devices in the Development department in support of the department's objectives to provide goods and services that meet customer requirements for quality, quantity, and timeliness.
The primary role of the R&D Engineer is to lead project deliverables and lead technical reporting of such deliverables to customers on time and on budget to meet customer objectives, and therefore bring projects to successful conclusions.
For Your Benefits:
Competitive salary
Billable overtime, or can be taken as additional PTO
Medical insurance (BCBS): Eligible on first day of employment
HSA-eligible medical plans
Dental insurance
Company-paid Vision, Life, and Long and Short-Term Disability insurance
401k safe harbor retirement plan
(18) days of Paid Time Off
Voluntary Life
TeleDoc program
Identity protection
Tuition Reimbursement
Paid time off for community outreach and volunteering
Essential Duties and Responsibilities:
Develop and engineer disposable medical devices from concept to production
Hands-on product and process development of catheters and other disposable products
Design devices in SolidWorks and build prototypes in a laboratory environment
Design, prototype, and construct catheters, catheter-based delivery systems, and other disposable devices for disciplines ranging from cardiology and neurology to urology
Acquisition, set up, and, installation qualification of new equipment, including the creation of PM procedure as necessary
Support of equipment maintenance, as appropriate per skills and knowledge
Support or perform equipment re-entry to line use
Communicate to the customer any issues and the status of the project
Prepare and support product development and quality planning (project schedule, resources, budgets, etc.)
Participate in the quotation process for projects
Develop feasibility and reliability testing plans for catheter systems, including the development and validation of accurate in-vitro and in-vivo models and methods
Develop pilot and manufacturing equipment and procedures for devices
Assess feasibility of processes and support manufacturing with validation plans and time studies
Support product manufacturing until project is fully transitioned to production
Manage and assist with verification and validation activities and documentation
Collaborate with outside vendors on the sourcing of catheter materials, components, and processing
Prepare documentation to support quality system for design functions (project plans, concept document, FMEA, design input, test results, drawings, etc.)
Complete activities as project phase checklists
Engage and handoff activities to manufacturing engineering
Support customer complaints
Lead design changes to existing product lines as necessary
Review document changes in manufacturing for impact on design intent
Demonstrate understanding of the D&D process by showing independence by recommending project direction and initiating project tasks to meet deliverables
Demonstrate competence of product development by communicating status and recommendations to customers
Gain customer satisfaction through adequate communication
Minimum Qualifications (Knowledge, Skills, Abilities):
BS or MS in Biomedical or Mechanical Engineering is required
1-5 years of experience with design and development of medical devices
Experience with FDA CFR 820 and ISO 13485 regulations
Strength in problem-solving and decision-making
High energy level, attention to detail and a sense of urgency
Computer skills including MS office, SolidWorks or alternative CAD program
Experience with project management is highly preferred to plan and conduct complex development projects
Skills with prototyping and materials knowledge for medical devices
Proficient customer interaction skills
Medical Murray is an equal-opportunity employer.
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