×
Register Here to Apply for Jobs or Post Jobs. X

Sr. R&D Engineer

Job in Tempe, Maricopa County, Arizona, 85280, USA
Listing for: BD (Becton, Dickinson and Company)
Full Time position
Listed on 2026-06-01
Job specializations:
  • Engineering
    Biomedical Engineer, Quality Engineering
Job Description & How to Apply Below
Position: Sr. R&D Engineer I
We are the people who give possibilities purpose

BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

This position works cross-functionally to lead research and development efforts of complex medical devices. The position designs, develops and implements new products, focusing on project planning, innovative medical device design, prototype development, testing characterization, analysis and reporting.

Essential /

Key Job Responsibilities (including supervisory and/or fiscal):

* Design:
Designs, develops and implements new products and processes of a medical device, translating intangible design inputs into tangible engineering specifications and drawings. Makes and presents engineering decisions. Participates and leads cross-functional teams in the design of a medical device. Contribute ideas and/or generate intellectual property submissions.

* Process Development: develops new processes by understanding key process inputs and outputs, using statistic methods such as DOE as appropriate. Develops new process equipment and tooling, including specification development, vendor selection and negotiation.

* Documentation: write and review product development plans, design reviews, technical documents and reports. Prepares and approves verification and validation protocols and reports. Develops and implements procedures/policy.

* Test Method Development: develop new engineering test methods and clinically relevant simulated use test methods in conjunction with R&D technicians; prepare and assist in the validation of test methods.

* Testing: conduct engineering and competitor evaluations, and development unit testing. Plan, develop, execute and manage verification and validation activities for new products and processes.

* Training: train technicians and engineers on new design and process development as well as new test methods.

* Supervisory/mentoring/coaching:
Mentor/coach R&D technicians and engineers through New Product Development activities. May supervise or manage technicians, engineers or supervisors.

* Fiscal:
Creates, controls, manages a project budget (expense and/or capital expenditure). Create and critique engineering cost analysis.

Other Responsibilities may include, however are not limited to:

* Support Manufacturing, Quality, Regulatory & R&D to ensure systems are compliant with all internal and external guidelines.

* Support/lead design and process root cause analysis and support non-conforming product and complaint investigations.

Required Qualifications:

* B.S. degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering or other related engineering discipline

* 6-9 years of industrial experience in R&D or process development

* Alternative:
Masters degree plus 4-6 years experience

* Alternative:
Ph.D. degree with 3-4 years experience

* Demonstrated hands-on technical aptitude

* Experience in process validation (IQ, OQ and PQ)

* Ability to write protocols and reports for verification and validation activities

* Ability to create and execute project plans

* Ability to lead cross-functional teams

* Basic tooling, design, and drafting knowledge

* Excellent oral and written communication skills

* Ability to analyze data, interpret results, and write reports

* Proficiency in statistical software

* Ability to travel ~ 25%, both domestic and internationally, as needed.

Preferred Qualifications:

* Masters degree in relevant engineering discipline

* Preferably experience in medical device or regulated FDA/QSR and ISO environment

* Knowledge of cGMP (current Good Manufacturing Practices) and GLP (Good Laboratory Practices)

* Biomedical Engineering or Bioengineering degree is preferred

* Training in Six Sigma or Design for Six Sigma

Physical Demands:

While performing the duties of this job, the employee is regularly required to stand, walk, sit, use sight, and use hands to manipulate, handle or feel objects, tools, controls, and office equipment. The employee frequently is required to verbally communicate with other associates. The employee is occasionally required to reach with hands and arms and stoop, kneel or crouch.

Work Environment:

While performing the duties of this job, the employee may be in an open cubicle environment. Candidate must be able to work in a team-oriented, fast-paced environment. BD is an affirmative action, equal opportunity employer that values and actively seeks diversity in the workforce. On occasion the employee may work in a preclinical setting like an animal lab, cadaver lab or attend clinical case observations.

This job description is intended as a summary of the primary responsibilities of and qualifications for this position. The job…
Position Requirements
5+ Years work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary