R&D Engineer II – BD (Tissuemed Ltd)
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As the R&D Engineer II, your primary focus is to support the development, optimisation, implementation, and validation of components and elements of a medical device. You will perform hands‑on testing, process development, documentation, and collaboration with cross‑functional teams in R&D, Quality, Operations, and Regulatory Affairs.
Job Description
BD is one of the largest global medical technology companies in the world, advancing health through innovative solutions. A career at BD offers learning opportunities, an inclusive culture, and the chance to shape the future of healthcare.
Main Responsibilities
* Design components, translating design inputs into specifications and drawings; select materials, processes, vendors; evaluate against standards and use scenarios; build test parts for evaluation.
* Process Development: develop and optimise processes using statistical methods; support new process equipment and tooling development, including specification, vendor selection, negotiation.
* Documentation: prepare work instructions and SOPs; write technical documents and reports; prepare raw material specifications; assist in verification and validation protocols and reports.
* Test Method Development: develop new engineering test methods and clinically relevant simulated use methods; assist in validation.
* Testing: perform lab bench testing, conduct engineering and competitor evaluations, unit testing, and verification/validation activities.
* Training: train technicians on new designs, processes, and test methods; conduct new process development training with operations and QA.
* Supervisory/mentoring: mentor R&D technicians through new product development activities, materials/inventory control.
Other Responsibilities
* Assist Manufacturing, Quality, Regulatory, and R&D in ensuring system compliance with internal and external guidelines.
* Assist in design and process root‑cause analysis and support non‑conforming product and complaint investigations.
About You
* B.S. in Mechanical, Biomedical, Chemical Engineering or related discipline (Biomedical Engineering preferred).
* Up to 3 years of industrial R&D or process development experience, preferably in regulated FDA/QSR & ISO environment.
* Hands‑on technical aptitude; experience in process validation (IQ, OQ, PQ); ability to write protocols and reports.
* Excellent oral and written communication skills.
* Ability to work in cross‑functional teams and analyse data, interpret results, write reports.
* Proficiency in statistical software (advantage).
* Knowledge of cGMP, GLP (advantage); training in Six Sigma or Design for Six Sigma (advantage).
Salary: €43,300.00 – €73,600.00 EUR annual (location-based).
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 status, domestic or civil union status, familial status, sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally‑protected characteristics.
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