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 MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job Description
Job Summary:
This position supports product leadership and risk management of new product development and sustaining activities for combination products . The role may include aspects of manufacturability, scalability, manufacturing transfer and post launch sustainability of combination products.
This job description is intended as a summary of the primary responsibilities of and qualifications for this position. The job description is not intended as inclusive of all duties an individual in this position might be asked to perform or of all qualifications that may be required either now or in the future.
Job Responsibilities:
Technical leadership skills including an understanding of medical device operations (e.g., medical device manufacturing, process development, quality assurance)
Leads development of risk assessments and test methods
Leads component qualifications, design validation / verification and process validation
Leads product investigations
Ability to make and present risked based decisions
Assess product changes against product design
Supports translation of design inputs into manufacturing control plans
Develop and implement procedures to comply with corporate and industry standards.
Coordinates and/or directs all aspects of product development activity related to a product line
Quality engineering representation on Product Development Teams to design, develop, and implement new products and processes for a medical device, translating intangible design inputs into tangible engineering specifications and test plans
Quality engineering representation on Design Review Teams
Prepare and present project updates and technical discussions
Participate in project planning, budgeting, scheduling, and tracking
Support internal and external supplier audits
Provide support to the regulatory department in writing technical submissions
Comply with company procedures and policies, government regulations
Ability to travel for business, project, and issues approximately up to 25% of time.
Other duties and projects, as assigned
Education and Experience:
BS in Engineering
Minimum of five years’ experience in engineering or Quality engineering experience within the medical device, pharmaceutical, or equivalent industry
Pharmaceutical or combination product experience preferred
Knowledge and Skills:
Knows how products are used and impact the user(s) so that risk can be managed effectively
Apply Quality Engineering tools (Sampling Plans, Root Cause Analysis, Statistics, etc.)
A bility to lead creation of risk management files
Ability to develop solutions with business impact
A dvanced statistical and risk assessment techniques
Working knowledge of test method (development and validation), equipment qualifications, process and design validation, risk assessment techniques, and component qualification methodologies
Ability to make and present risk-based decisions
Strong interpersonal skills
Ability to analyze and optimize manufacturing and quality systems Product, design & prototyping
Ability to create and provide trainin
Problem solving ability
Ability to create, review and coordinate test protocols and reports
Ability to generate engineering proposals
Oral and written presentation skills
Ability to Lead cross functional teams
Understanding of regulatory requirements including ISO 13485, ISO 14971, 21 CFR 210/211/820
Preferred Qualifications:
Quality Engineering Certification (ASQ) or equivalent
Why Join Us? To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
To learn more about BD visit bd.com .
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.
Required Skills
Optional Skills
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Primary Work Location USA AZ - Tempe Headquarters
Additional Locations
Work Shift
Requirements
Must-haves
We are the people who give possibilities purpose
Technical leadership skills including an understanding of medical device operations (e.g., medical device manufacturing, process development, quality assurance)
Leads development of risk assessments and test methods
Leads component qualifications, design validation / verification and process validation
Leads product investigations
Ability to make and present risked based decisions
Assess product changes against product design
Supports translation of design inputs into manufacturing control plans
Develop and implement procedures to comply with corporate and industry standards.
Coordinates and/or directs all aspects of product development activity related to a product line
Quality engineering representation on Design Review Teams
Prepare and present project updates and technical discussions
Participate in project planning, budgeting, scheduling, and tracking
Support internal and external supplier audits
Provide support to the regulatory department in writing technical submissions
Comply with company procedures and policies, government regulations
Ability to travel for business, project, and issues approximately up to 25% of time.
Other duties and projects, as assigned
BS in Engineering
Minimum of five years’ experience in engineering or Quality engineering experience within the medical device, pharmaceutical, or equivalent industry
Knows how products are used and impact the user(s) so that risk can be managed effectively