R&d/product DVL Engineer
Consider a career with us
TE Connectivity (NYSE: TEL) is a $12 billion global technology leader. Our connectivity and sensor solutions are essential in today's increasingly connected world. We collaborate with engineers to transform their concepts into creations redefining what's possible using intelligent, efficient and high-performing TE products and solutions proven in harsh environments. Our 72,000 people, including over 7,000 engineers, partner with customers in over 150 countries across a wide range of industries. We believe EVERY CONNECTION COUNTS www.TE.com.
These positions are based in our Creganna Medical, Plymouth Minnesota facility.
Overview
The Research and Development Engineer is responsible for providing engineering knowledge, skill, and ability to handle such tasks as: project management, engineering design, prototyping development, gathering of pertinent back ground information, and leading project and design teams from conception through commercial launch of medical devices. Additionally, the Research and Development Engineer will be responsible for managing project costs, issuing quotes to customers, procuring material quotes, interacting with customers while ensuring full compliance to FDA QSR (21 CFR 820), and applicable ISO 13485 requirements.
Responsibilities & Qualifications
Will be responsible for establishing product requirements, concept prototyping, design and development (including verification and validation), risk/failure mode assessment, performance and safety testing.
Coordinate time and activities of others and/or serve as a project leader for cross-functional projects.
Maintains detailed documentation throughout all phases of research and development.
Reviews or coordinates outside vendor activities to support development.
Manages or develops technical solutions to design problems with vendors and in-house resources through design reviews, design audits, and prototype analysis.
Interface with customers and internal departments articulating team activities and progress.
Work closely with manufacturing engineering to improve process, procedure, and cost.
Excellent computer skills including Microsoft office (Word, Excel, PowerPoint) statistical software, Solid works or AutoCAD software.
Highly motivated with a sense of urgency in resolving quality issues relating to customer requirements and demands.
Possesses strong verbal and written communication skills.
Excellent time management skills. Demonstrated ability to complete timeline commitments.
Able to adapt to changing priorities and manage multiple initiatives concurrently in a fast-paced environment.
Proven track record for quality improvement initiatives.B.S. in Mechanical Engineering or Bachelor's Degree plus a minimum of seven (7) years experience in a related regulated medical device environment. Or a Master's Degree with 0-2 years of related work experience, or an equivalent combination of education and work experience.
EDUCATION AND/OR
Experience:
B.S. in Mechanical Engineering or Bachelor's Degree plus a minimum of seven (7) years experience in a related regulated medical device environment. Or a Master's Degree with 0-2 years of related work experience, or an equivalent combination of education and work experience.
. Apply now!Estimated Salary: $20 to $28 per hour based on qualifications.
TE Connectivity (NYSE: TEL) is a $12 billion global technology leader. Our connectivity and sensor solutions are essential in today's increasingly connected world. We collaborate with engineers to transform their concepts into creations redefining what's possible using intelligent, efficient and high-performing TE products and solutions proven in harsh environments. Our 72,000 people, including over 7,000 engineers, partner with customers in over 150 countries across a wide range of industries. We believe EVERY CONNECTION COUNTS www.TE.com.
These positions are based in our Creganna Medical, Plymouth Minnesota facility.
Overview
The Research and Development Engineer is responsible for providing engineering knowledge, skill, and ability to handle such tasks as: project management, engineering design, prototyping development, gathering of pertinent back ground information, and leading project and design teams from conception through commercial launch of medical devices. Additionally, the Research and Development Engineer will be responsible for managing project costs, issuing quotes to customers, procuring material quotes, interacting with customers while ensuring full compliance to FDA QSR (21 CFR 820), and applicable ISO 13485 requirements.
Responsibilities & Qualifications
Will be responsible for establishing product requirements, concept prototyping, design and development (including verification and validation), risk/failure mode assessment, performance and safety testing.
Coordinate time and activities of others and/or serve as a project leader for cross-functional projects.
Maintains detailed documentation throughout all phases of research and development.
Reviews or coordinates outside vendor activities to support development.
Manages or develops technical solutions to design problems with vendors and in-house resources through design reviews, design audits, and prototype analysis.
Interface with customers and internal departments articulating team activities and progress.
Work closely with manufacturing engineering to improve process, procedure, and cost.
Excellent computer skills including Microsoft office (Word, Excel, PowerPoint) statistical software, Solid works or AutoCAD software.
Highly motivated with a sense of urgency in resolving quality issues relating to customer requirements and demands.
Possesses strong verbal and written communication skills.
Excellent time management skills. Demonstrated ability to complete timeline commitments.
Able to adapt to changing priorities and manage multiple initiatives concurrently in a fast-paced environment.
Proven track record for quality improvement initiatives.B.S. in Mechanical Engineering or Bachelor's Degree plus a minimum of seven (7) years experience in a related regulated medical device environment. Or a Master's Degree with 0-2 years of related work experience, or an equivalent combination of education and work experience.
EDUCATION AND/OR
Experience:
B.S. in Mechanical Engineering or Bachelor's Degree plus a minimum of seven (7) years experience in a related regulated medical device environment. Or a Master's Degree with 0-2 years of related work experience, or an equivalent combination of education and work experience.
. Apply now!Estimated Salary: $20 to $28 per hour based on qualifications.
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