Join to apply for the Senior R&D Engineer I role at BD Nogales Norte
Job Description Summary
As the Senior R&D Engineer you will work cross‑functionally to lead research and development efforts of complex medical devices. You will design, develop and implement new products, focusing on project planning, innovative medical device design, prototype development, testing characterisation, analysis and reporting.
BD – About the Company
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 MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.
Main Responsibilities Will Include
* 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.
About You
* B.S. degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering or other related engineering discipline. Biomedical Engineering or Bioengineering degree preferred.
* 6+ years of industrial experience in R&D or process development, preferably in medical device or other regulated FDA/QSR and ISO environment.
* Demonstrated hands‑on technical aptitude.
* Experience in process validation (IQ, OQ and PQ), writing protocols and reports to support verification and validation activities for product commercialization; ability to execute validation.
* Ability to create and execute project plans and lead cross functional teams.
* Basic tooling, design and drafting knowledge.
* Excellent oral and written communication skills.
* Ability to analyse data, interpret results, and write reports.
* Proficient in statistic software.
* Training in Six Sigma or Design for Six Sigma.
* Knowledge of cGMP and GLP is a distinct advantage.
Salary Range
€73,500.00 - €125,000.00 EUR Annual
Equal Opportunity Employer
Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally‑protected characteristics.
#J-18808-Ljbffr