New · posted Oct 27
Becton Dickinson · Medical Devices
Sr. Quality Engineer
- Covington, GA
- On-site
- Full-time
- Senior & Principal
What you need
Required Qualifications
- Bachelor's degree in Chemical Engineering or a closely related engineering disciplines
- 3 years of experience in a Quality Engineering role within the medical device industry.
- Demonstrated experience with design controls, risk management (ISO 14971), and CAPA processes.
Required Skills
Optional Skills
Skills and Knowledge
- Demonstrated knowledge of chemical processes, materials, process validation, manufacturing operations, and continuous improvement methodologies.
- Strong understanding of FDA Quality System Regulations (21 CFR Part 820) and ISO 13485.
- Proficiency in statistical analysis techniques and quality tools (e.g., Minitab, SPC, FMEA).
- Excellent problem-solving, analytical, and critical thinking skills.
- Strong written and verbal communication skills, with the ability to effectively interact with all levels of the organization.
- Ability to work independently and as part of a cross-functional team in a fast-paced environment.
Preferred Qualificationsnice to have
- ASQ certifications (e.g., CQE, CSSBB)
- Experience with Class II or III devices
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.
What you'll do
- Develop, implement, and maintain quality plans, procedures, and specifications to ensure compliance with regulatory requirements and industry standards, including FDA QSR and ISO 13485.
- Support product development through design control activities such as design reviews, risk assessments, and verification and validation testing to ensure product quality, safety, and effectiveness.
- Investigate product nonconformances, customer complaints, and manufacturing deviations using root cause analysis methodologies, and drive effective Corrective and Preventive Actions (CAPA).
- Plan and execute internal and external audits to evaluate quality system compliance and identify opportunities for continuous improvement.
- Partner with suppliers to support qualification, performance monitoring, and ongoing supplier quality management activities.
- Analyze quality metrics and trends, prepare reports, and communicate quality performance insights to leadership and key stakeholders.
- Lead and contribute to continuous improvement initiatives utilizing Lean, Six Sigma, and other quality tools and methodologies.
- Deliver training, coaching, and guidance to cross-functional teams on quality systems, compliance requirements, and best practices.
- Collaborate closely with R&D, Manufacturing, Regulatory Affairs, and other business functions to embed quality throughout the entire product lifecycle.
- Support regulatory submissions and assist in responding to regulatory agency inquiries as needed.
Pay
Becton Dickinson didn't publish pay for this role
See what similar roles pay on Regulatory Jobs, or try the salary calculator.
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.
Where you'll work
Covington, GAOn-siteOpen in Maps (opens in a new tab)
More jobs in Covington, GASchedule and working conditions
Days
Hours
US BD 1st Shift 8am-5pm (United States of America)
Primary Work Location
USA GA - Covington BMD
From the posting
About BD
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.
Equal opportunity, accessibility and legal noticesBecton Dickinson's statements, word for word
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.
Job intelligence
The context around this role
Live data · October 28, 2026
Salary intelligence
How the pay compares
Senior & Principal roles in the US323 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| All US (middle half) | $104,000 | $122,000 | $142,250 |
Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 28, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 961 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not BD's own promotion track.
Career resources on Quality Assurance
Skills DNA
What this role leans on
How many of the posting's 24 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Quality systems and risk10
- Collaboration and leadership7
- Lab testing and methods6
- GMP and compliance4
- Validation and qualification3
- Documentation and SOPs2
- Investigations and CAPA2
- Regulatory submissions1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
- ISOISO 14971(official source, opens in a new tab)Risk management for medical devices
Company hiring pulse
BD on Regulatory Jobs
- 89
- Open roles
- 82
- Distinct roles
- 20
- Locations
By discipline
- Quality68 76%
- Regulatory19 21%
- Compliance & Safety2 2%
By level
- Senior & Principal44 49%
- Associate & Specialist27 30%
- Manager15 17%
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Sr. Quality Engineer at BD
Open until filled.