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$106k–$169k/yr
Full-time
bachelor degree, postgraduate degree
Total Rewards program, Compensation and benefits programs, Reward and recognition opportunities
Posted 3d ago
~40 hrs/week
Responsibilities
The Senior Quality Engineer leads design assurance and development activities while ensuring compliance with regulatory requirements and quality systems. They also investigate complex manufacturing quality issues and implement engineering solutions to optimize product development and manufacturing processes.
Requirements
Candidates must hold a Bachelor's degree in an Engineering or Scientific field with at least 4 years of experience, or a Master's with 2 years, or a Ph.D. with 1 year. Hands-on experience with Design Assurance and working within a highly regulated industry is required.
Full job description



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
The Sr. Quality Engineer role will apply knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and quality systems/procedures to optimize product development, internal and external device manufacturing, and device distribution.
How you will make an impact:
Leads design assurance and development activities (i.e., requirement development, risk assessment, engineering study, feasibility testing, drawing review, etc.) for New Product Development programs
Provides engineering solutions in the areas of Quality Assurance, Design Control, Risk Management, and Statistical Techniques.
Develop, update, and maintain technical content of risk management files
Collaborates cross-functionally (eg. R&D, Mfg/Ops, Regulatory) to help facilitate the successful execution of the NPD process and launching of robust products
Develop and validate complex experiments and tests (including writing and executing protocols) to create, validate, and improve products (including evaluation of source materials and suppliers) and manufacturing processes/methods based on engineering principles; analyze results, make recommendations, and develop reports.
Investigate complex manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports.
Lead identification, development, and optimization of design verification activities and complex manufacturing processes using engineering methods (e.g., Six Sigma and Lean manufacturing tools) for design for manufacturing and continuous process improvement initiatives. Identify opportunities & implement solutions for re-design/design of complex equipment, new technologies (including automation and software), tools, fixtures, etc. to
Assigns tasks; gives instruction to technicians on conducting tests; trains technicians and less seasoned engineers and provides feedback; and may coordinate engineer work.
Other incidental duties assigned by Leadership
What you’ll need (Required Qualifications):
Bachelor's Degree in in Engineering or Scientific field , 4 years experience including either industry or industry/education Required or Master's Degree or equivalent in in Engineering or Scientific field , 2 years experience including either industry or industry/education Required or Ph.D. or equivalent in in Engineering or Scientific field , 1 years experience including either industry or industry/education Required
Hands-on experience with Design Assurance, including Design Controls, Design Freeze (or pre-design testing), Design Verification & Validation, and/or Design Test Method Development
Experience working within a highly regulated industry
What else we look for (Preferred):
Knowledge of and experience with Risk Management/Usability Engineering and authoring risk management documents.
Demonstrated technical leadership (i.e., solving complex problems; implementing a process or Quality improvement; piloting/creating new methodologies)
In-depth working knowledge and understanding of statistical techniques
Ability to read and interpret drawings
Ability to translate technical information to all levels of the organizations
Test Method Development and Validation Experience
Working knowledge of the Domestic and International regulatory requirements of Medical Device regulations (FDA 21 CFR 820, ISO 13485, ISO 14971, ISO 62366; and other applicable regulatory requirements)
Knowledgeable with MDR regulations
Strong technical writing skills
Ability to manage competing priorities in a fast paced environment
Work is performed independently while exercising considerable latitude in making significant decisions
Must be able to work in a team environment, including frequent inter-organizational and outside customer contacts
Represents organization in providing solutions to difficult technical issues associated with specific projects
Develops technical solutions to complex problems which require the regular use of creativity
Uses best practices and knowledge of internal or external business issues to improve products/services or processes
Typically resolves complex problems or problems where precedent may not exist
Travel Requirements: % not specified, but travel has occurred in the past on an as-needed basis for project continuity
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.
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
.
Primary Work Location
USA CA - Irvine Laguna Canyon
Additional Locations
Work Shift



At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs. You can learn more on our career site under "Our Commitment to You."
Our salary or hourly rate ranges reward associates fairly and competitively. We regularly review these ranges and factors, such as location, contribute to the range displayed.
Our pay is based on the role and the necessary skills and education to perform it successfully. The salary or hourly rate offered is determined by the role's specific requirements, including any applicable step rate pay system at the work location. Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location which may also affect the workplace arrangement of the role.
BD is the world's largest manufacturer and seller of medical equipment.
Industry
Medical Equipment Manufacturing
Company size
501-1,000 employees
Headquarters
纽约
LinkedIn followers
6,368
BD is one of the world's largest medical technology companies that produce and sell medical equipment, medical systems and reagents, dedicated to improving human health around the world.
BD focuses on improving drug treatment, improving the quality and speed of diagnosis of infectious diseases, and promoting the research and discovery of new drugs and vaccines.
BD has strong research and development capabilities to fight many of the world's most intractable diseases.
Founded in New York in 1897, the company is headquartered in Franklin Lake, New Jersey, USA and employs more than 25000 people in about 50 countries around the world.
The company's clients include medical institutions, life sciences research institutes, clinical laboratories, industrial units and the general public.