Quality Engineer 1, EU MDR

BD

Sandy (UT)

On-site

USD 90,000 - 110,000

Full time

28 hours ago
Be an early applicant

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

BD is a global medical technology company seeking a Quality Assurance professional to develop test requirements, write protocols, and conduct validation studies. The role supports on-site manufacturing and NPD, ensuring regulatory compliance and continuous improvement across processes.

The position emphasizes collaboration with R&D, Regulatory, Manufacturing, and Supply Chain, and requires the ability to lead investigations and present technical updates. On-site presence is required in Utah.

Qualifications

  • Bachelor degree in STEM (Science, Technology, Engineering, Math).
  • The incumbent must demonstrate the potential ability to perform the essential functions of the job.

Responsibilities

  • Develops physical and functional test requirements to assure specs and regs are met.
  • Writes, reviews, and approves protocols, reports, and data.
  • Conducts testing outlined in protocols and test methods.
  • Executes validation studies on equipment and processes and investigates complaints.
  • Follows company procedures and regulatory requirements.
  • Analyzes design, process, and test data.
  • Prepares and presents project updates and technical discussions.
  • Leads continuous improvement initiatives.

Education

Bachelor in STEM

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.

Responsibilities
  • Develops physical and functional test requirements to assure specifications and regulations are met.
  • Writes, reviews, and approves protocols, reports, and data.
  • Conducts testing outlined in protocols and test methods.
  • Executes validation studies on equipment and processes, and conducts and/or participates in complaints investigations.
  • Understands and follows company procedures and regulatory requirements.
  • Participates in and provides input to training on department & division procedures, and policies.
  • Analyzes design, process, and test data.
  • Prepares and presents oral and written project updates and technical discussions.
  • Develops and implements procedures to provide easy to follow instructions.
  • Develop sampling plans by applying attribute, variable, and sequential sampling methods. Develop local procedures, Test Methods, and standards.
  • Develop and implement Statistical Process Control.
  • Leads investigations related to quality problems.
  • Ability to define and manage risk-management plan, risk assessment and risk-control tools.
  • Facilitate or independently lead non-conforming product investigations, including corrective/preventive actions and product remedial actions.
  • Responsible for systems assurance including documentation, testing and inspection, and product and process development.
  • Will support Manufacturing, New Product Development, and Regulatory (as applicable) to ensure systems are in compliance with internal and external guidelines and regulations.
  • Identify and lead product and systems continuous improvement initiatives.
  • Communicate effectively at all levels within Quality, as well as cross-functionally with R&D, Regulatory Affairs, Manufacturing, Supply Chain, Customer Service, Marketing, and other functions as necessary.
  • Execute design controls and analyzes design inputs.
  • Will participate in internal/external audits.
Minimum Qualifications
  • Bachelor degree in STEM (Science, Technology, Engineering, Math)
Preferred Qualifications Include
  • Candidates with an engineering degree.
  • Candidates that have engineering experience within the medical device or equivalent regulated industry.
  • The incumbent must demonstrate the potential ability to perform the essential functions of the job as outlined in the duties and responsibilities.

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.

For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

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 https://bd.com/careers.

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.

Primary Work Location

USA UT - Salt Lake City BAS

Additional Locations

USA UT - Sandy

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Quality Engineer 1, EU MDR
Quality Engineer 1, EU MDR

BD • Salt Lake City (UT)

On-site
USD 70,000 - 110,000
Quality Engineer 1, EU MDR
Quality Engineer 1, EU MDR

Becton, Dickinson and Company • Salt Lake City (UT)

On-site
USD 85,000 - 120,000
Intern, R&D Engineering
Intern, R&D Engineering

Becton, Dickinson and Company • Salt Lake City (UT)

On-site
USD 20,000 - 26,000
Quality Engineer I
Quality Engineer I

Becton, Dickinson and Company • Salt Lake City (UT)

On-site
USD 70,000 - 110,000
Engineering Lab Technician 2
Engineering Lab Technician 2

BD • Salt Lake City (UT)

On-site
USD 60,000 - 90,000
R&D Engineering Intern - MedTech, On-Site, Fast-Paced
R&D Engineering Intern - MedTech, On-Site, Fast-Paced

BD • Salt Lake City (UT)

On-site
USD 20,000 - 26,000
Engineering Lab Technician 2
Engineering Lab Technician 2

Becton, Dickinson and Company • Salt Lake City (UT)

On-site
USD 50,000 - 80,000
Sr. Quality Engineer
Sr. Quality Engineer

Becton, Dickinson and Company • Covington (GA)

On-site
USD 80,000 - 110,000
Sr. Quality Engineer
Sr. Quality Engineer

BD • Covington (GA)

On-site
USD 85,000 - 110,000
Sr. Design Quality Engineer
Sr. Design Quality Engineer

BD • Covington (GA)

On-site
USD 120,000 - 180,000
On-site work requirement
Collaboration across sites