Job Description Summary
As the R&D Manager
you will coordinate department activities during product development and manage assigned personnel.
You will design, develop and implement new products focusing on project planning, innovative medical device design, prototype development, testing characterisation, analysis and reporting.
About BD
BD is one of the largest global medical technology companies.
Advancing health is our purpose, and we foster an inclusive, growth-centered culture.
We welcome imagination and drive to reinvent health.
Why Join Us?
Learn, work alongside leaders, shape BD's trajectory and leave a legacy.
Discover a culture where you can grow and thrive.
Main Responsibilities
Product Development: Direct all product development activity related to a product line, integrating RA, QA/QE, Operations, Clinical, Marketing, Sales and Packaging Engineering.
Project Management: Create and track project schedules, plans and budgets for new product development, ensuring department priorities are met.
Design to Manufacturing Transfer: Propose and facilitate selection of manufacturing location and oversee new product transfer.
Design: Oversee the design, development and implementation of new medical devices and processes.
Process Development: Lead R&D project leaders, engineers and manufacturing teams in developing new processes.
Documentation: Review product development plans, design reviews, technical documents and reports; approve verification and validation protocols.
Test Method Development: Oversee development of clinically relevant test methods.
Testing: Oversee planning and execution of qualification activities for new products and processes.
Training: Train new product development teams on new design and process development procedures.
Supervisory/Coaching: Mentor R&D teams, conduct performance reviews, recommend salaries and promotions.
Fiscal: Create, control and manage a department budget; review and analyse costs to implement cost improvements.
Other Responsibilities
Support Manufacturing, Quality, Regulatory and R&D to ensure systems are compliant with all internal and external guidelines.
Support design and process root cause analysis and support non-conforming product and complaint investigations.
About You
B.S. degree in Mechanical, Biomedical, Chemical Engineering or related discipline; Biomedical Engineering preferred.
8+ years industrial R&D or process development experience in regulated FDA/QSR and ISO environment.
Knowledge of development, manufacturing and quality system requirements for medical devices.
Experience in process validation (IQ, OQ, PQ) and writing protocols and reports.
Ability to create and deliver project plans and lead multifunctional teams.
Excellent oral and written communication skills.
Strong analytical ability and proficiency in statistical software.
Six Sigma or Design for Six Sigma training.
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, citizenship status, marital or domestic status, family status, sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
Salary Range
€73,****** - €125,****** EUR Annual
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