Job ID R-412454 Date posted 09/16/2021

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 Description Summary

Job Description

Be part of something bigger!

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. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

The Staff Quality System Specialist I is responsible for assuring quality standards and regulatory compliance are consistent with Corporate and Division Policies, Government Regulations, International Standards and Standards of the Medical Device Industry. The Staff Quality Systems Specialist I will be supporting the continued development, improvement and implementation of the Quality Systems within BD Medication Delivery Solutions (MDS) Business Unit. This position reports to the Senior Manager, Quality Systems.

Essential Responsibilities:

  • Maintains and improves the Franklin Lakes and WW MDS Quality System for assigned elements.

  • Implements quality system elements required for compliance to the new EU MDR (Medical Device Regulation) requirements.

  • Collaborates with cross-functional partners to seek their input into the development of policies and procedures, Quality System manuals, and their support in addressing Quality Issues.

  • Facilitates cross-functional interaction and communication between Quality, Regulatory Affairs, R&D, Regulatory Affairs, Manufacturing, Operations, Sales, and Marketing and other applicable teams to support in Quality System improvement and compliance.

  • Participates and supports internal and external regulatory site visits, inspections, and audits. Including ensuring that pre and post-inspection activities are completed including scheduling, record review, training, logistics, etc. in Franklin Lakes and worldwide.

  • Assists with FDA, MDSAP, NB, Corporate and other regulatory, external, and internal audit readiness and processes harmonization globally in Franklin Lakes and worldwide.

  • Applies quality and/or standard-setting body requirements to develop solutions, control and/or maintain technical documents and/or Quality Systems.

  • Trains, develops, and provides technical guidance to other associates.

  • Actively participates in quality guidance and helps project & quality network teams for process improvement, standardization initiatives, and continuous improvement activities

  • May serve as a representative on BD Corporate Quality Networks, being responsible for implementing Network objectives at sites worldwide.

  • Completes projects/other duties as assigned.


  • Consistent understanding of the application of quality systems to the medical device industry.

  • Expert knowledge of US and International regulations and standards that apply to the medical device industry including FDA Quality System Regulations, ISO 13485, MDD, EUMDR, Canadian MDR, Japan PMDA, AVISA and TGA requirements.

  • Excellent communication skills.

  • Experience with external audit.

  • Experience with change management.

  • Program management experience.

  • Experience with remediation.

  • Ability to set and deliver to specific goals and targets.

  • Ability to perform multiple tasks and prioritize workload.

  • Effective analytical, technical, and problem-solving skills.

  • Effective meeting and presentation skills.

  • Effectively manage conflict.

  • Ability to work in or direct teams to obtain results.

  • Self-motivated /directed.

Education and Experience:

  • Bachelor’s Degree plus 5-10 years of experience or a combination of equivalent education and relevant experience

  • Minimum 5 years of experience with US and International regulations and standards that apply to the medical device industry including FDA Quality System Regulations, ISO 13485, MDD, EUMDR, Canadian MDR, Japan PMDA, AVISA and TGA requirements.

  • Medical device industry experience

Why join us?

A career at BD means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our associates can fulfill their life’s purpose through the work that they do every day.

You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program — which includes competitive pay, benefits, continuous learning, recognition, career growth, and life balance components — is designed to support the varying needs of our diverse and global associates.

To learn more about BD visit

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.

Primary Work Location

USA NJ - Franklin Lakes

Additional Locations

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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
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  • 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.

BD is unique in how fully dedicated it is to a specific disease state. It makes it clear how the work we do directly impacts the daily lives of the patients we serve.

Eric Rainis
Senior Director Quality Management

To know that our products touch 30 million people with diabetes around the globe is powerful and fuels our teams to deliver best in class products to them each and every day.

Bridget Bagnato
VPGM Injection

It is inspiring to see BD products to be used globally to advance human healthcare.

Yang Zeng
Manager Medical Laboratory



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