
Technologist, R&D
Type
Full time
Category
Engineering
Location
Job reference
Req-47205
Posted for
4 days ago
Innovation starts from the heart. At Edwards, we put patients first. We invest a significant proportion of our revenue towards research and development to drive and develop groundbreaking medical innovations for structural heart disease and critical care.
Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient’s unmet clinical needs. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
This Technologist, R&D has the opportunity to join an early-stage Transcatheter Mitral Valve Replacement (TMVR) program and support critical activities in designing a novel implant. If you’re an exceptional engineering technician professional with significant experience and a heart for solving complex challenges, join our team and help us improve patients’ lives through the development of a TMVR therapy from the ground up.
How you’ll make an impact:
Support a wide range of engineering activities such as test, check out, modification, fabrication and assembly; may formulate and propose technical solutions
Design and build complex prototypes, sub-assemblies, and prepare feasibility test units, samples, and/or chemical solutions; may include making material recommendations
Perform operational test and identify failure modes on systems and equipment and propose and implement technical solutions
May build prototypes for physician demonstration
Perform complex work using drawings, diagrams, written and verbal instructions, layouts or defined plans to perform testing, checkout, and trouble-shooting functions
Collect, document, and analyze test data
Operate all lab equipment including set-up, clean-up, break-down, and re-assembly
Train, coach, and guide lower-level employees on new procedures, assess work techniques and provide feedback to engineers on procedures
Generate reports and support recommendations for changes and improvements; may include presenting findings for review
Design and build complex fixtures, using sketches, CAD, etc
Perform test method development and validation for equipment and product designs
May create and modify drawings and procedures for fixtures, equipment, products, or processes
Independently problem solve and perform root cause analysis for a wide range of engineering activities
Characterize and assess design performance against predetermined requirements
May initiate ECRs (Engineering Change Request)
On time arrival to work, regular attendance without excessive absenteeism, and working a full 8 hour or longer work period
Other incidental duties (e.g. occasional photocopying or deliveries)
What you'll need (Required):
Associate's degree or technical degree/certificate and 4+ years of previous experience in an R&D Lab and/or medical device experience - OR –
6+ years of experience in an R&D Lab and/or medical device experience
What else we look for (Preferred):
Strong written and verbal communication, interpersonal, and relationship building skills
Problem solving methodology, root cause analysis, and GDP (Good Documentation Practices)
Strong computer skills, including usage of MS Office Suite; and CAD if applicable
Full understanding of equipment in a lab environment
Ability to perform complex troubleshooting
Ability to identify problems and relevant issues in complex situations, assessing using standard procedures
Ability to use a wider range of manufacturing, test, development or diagnostic equipment; use tools such measuring equipment
Ability to read and understand procedures, drawings, schematics and carry out assembly instructions
Knowledge and understanding of statistical techniques and procedures
Ability to utilize CAD/drafting software (if applicable)
Knowledge and understanding of ECR software systems (if applicable)
Ability to draft technical documents (i.e, manufacturing and testing procedures)
Knowledge of and adherence to Edwards Environmental Health and Safety and Quality guidelines as they relate to lab and/or clean room medical device manufacturing
Strict attention to detail
Must be able to work in an inter-departmental team environment, as well as with colleagues from other departments and represent organization to outside contacts, i.e., vendors
Ability to provide feedback in a professional, direct, and tactful manner
Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $61,000 to $86,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Job reference
Req-47205
Type
Full time
Category
Engineering
Location
Posted for
4 days ago
Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. Through breakthrough technologies, world-class evidence and partnerships with clinicians and healthcare stakeholders, our employees are inspired by our patient-focused culture to deliver life-changing innovations to those who need them most.
What we offer
