Be part of something bigger at BD. Here, you’ll help us continually improve how we do things every day; to be more efficient, more effective and better serve our customers. You’ll do this within an exceptional team all striving to make sure that everything we do complies with regulations and standards, not just because it’s the right thing to do, but because our products impact people’s quality of life. Here, you’ll put your compliance experience, high expectations and attention to detail to the very best use: advancing the world of health™. At BD, you can make a true difference of one.
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Job Type:
Full-Time -
Job Level:
Entry to Senior -
Travel:
Varies -
Salary:
Competitive -
Responsibilities
Job Description Summary
This position is responsible for performance of audits in support of the BD Quality Audit program.In this role, he/she is responsible for carrying out quality audits to support the various audit programs impacting BD sites.
In addition, he/she will work with the sites to ensure submitted objective evidence is compliant with domestic and international regulations, corporate standards, and local procedures.
He/she will maintain the audit database to monitor audit program metrics and prepare reports for management.
Job Description
We are the makers of possible
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.
Why join us?
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.
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 health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.
Become a maker of possible with us!
Our vision for our Quality Team at BD
In our Quality team, we collaborate on a large scale, focusing on making sure everything is correct, effective and efficient to bring the highest-quality and most competitive products and services to our customers and their patients.
About the role
As Staff Quality Auditor I, you will be responsible for the performance of audits in support of the BD Quality Audit program in the EMEA region and others as directed by the Associate Director, Quality & Regulatory Compliance, Quality Audits. We are the makers of possible 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 our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element across our global teams allows us to evolve continually. Join us and discover an environment where you’ll be supported to learn, grow and become your best self. Become a maker of possible with us.
Main responsibilities will include:
- Conducts Quality Audits to assure compliance with domestic and international medical device standards and regulations, local procedures, and corporate policies/procedures.
- Follows up with the auditee as required to compile information relating to the audits.
- Evaluates the adequacy of the provided evidence against the approved Audit Action Plan (AAP). In conjunction with management, develop plans to address inadequate AAP documentation when required.
- Maintains the audit system software database to record the status of all audits and associated actions.
- Provides periodic reports to management based on the audit statuses and defined metrics.
- Maintains a high degree of personal professional development through a combination internal and external training and participation in professional associations as appropriate.
- This individual’s primary responsibility will be to perform quality internal audits of the various location’s Quality management systems which may result in identification of compliance risks that need to be addressed by the business to improve its compliance position and influence the quality strategy by the management team.
- This individual will also be responsible for the execution of the department’s projects and strategic initiatives.
- This individual will be interacting with individuals at various levels of the organization across multiple sites in performing audits at these assigned locations including top management.
About you
- B.S. Engineering, Chemistry, Biology or equivalent discipline, advanced degree is preferred.
- One of the below certifications or equivalent: (Required)
- Certified Quality Auditor/ISO Lead Auditor Certified
- Certified Quality Engineer
- Certified Manager of Quality / Organizational Excellence
- Knowledge and experience in CAPA; Root Cause Investigation; Validation (Process, Test Method, Software, and Design); Environmental Monitoring; Sterilization (EtO, Irradiation)
- Exemplar Global ISO 13485 Lead Auditor Certification or equivalent (Preferred)
- Minimum 8- 10 years of work experience in the quality organization of a medical device and/or pharmaceutical company. Experience with warning letters and other regulatory actions is preferred.
- Minimum of 5+ years’ experience in auditing compliance with domestic and international regulations for medical devices or pharmaceuticals.
Click on apply if this sounds like you!
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of 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, or any other protected status.
To learn more about BD visit: https://bd.com/careers
Required Skills
Optional Skills
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Primary Work Location
GBR Winnersh - Eskdale RoadAdditional Locations
BEL Erembodegem - Dorp 86, BEL Olen, BEL Temse - Laagstraat, ESP Almaraz - Ctra. Nacional, ESP Barcelona, ESP Huesca - Fraga, ESP Malaga - Camino de Casabermeja, ESP Salamanca, ESP San Agustin del Guadalix, ESP Valencia - Paterna, ESP Zaragoza, GBR Crawley, GBR Leeds, GBR Plymouth - Belliver Industrial Estate, GBR Swindon - Dorcan, GBR WorthingWork Shift
Success Profile
What makes a successful Quality Professional at BD? Check out the top traits we’re looking for and see if you have the right mix.
- Ambitious
- Collaborative
- Goal-oriented
- Persuasive
- Results-driven
- Self-starter
Advancing the world of health™
BD is one of the largest global medical technology companies in the world and is advancing the world of health™ by improving medical discovery, diagnostics and the delivery of care. BD helps customers enhance outcomes, lower costs, increase efficiencies, improve safety and expand access to health care.