As a Coordinator 3 in Quality Document System Management at BD, you will play a critical role in maintaining and optimizing our quality documentation systems to ensure compliance with regulatory standards in the healthcare industry. This position offers the opportunity to contribute to innovative medical solutions while advancing your expertise in document control and quality assurance.

BD, a global leader in medical technology, is seeking a dedicated Coordinator 3 for Quality Document System Management to join our dynamic team in Warwick, Rhode Island. In this pivotal role, you will be responsible for overseeing the lifecycle of quality documentation, ensuring accuracy, accessibility, and compliance across all systems. You will collaborate with quality assurance, regulatory affairs, and operations teams to implement and maintain robust document control processes that support our mission of advancing healthcare.

Key responsibilities include reviewing and approving documentation for product development and manufacturing, conducting audits to verify system integrity, and training staff on best practices for document handling. You will also lead initiatives to streamline workflows, reduce errors, and enhance efficiency using state-of-the-art electronic document management systems. This position requires a proactive approach to identifying improvement opportunities and mitigating risks associated with non-compliance.

At BD, we value innovation, integrity, and inclusion. You'll work in an environment that fosters professional growth and offers exposure to cutting-edge medical technologies. If you have a passion for quality excellence and a commitment to patient safety, this role provides the platform to make a meaningful impact.

• Bachelor's degree in a related field such as Quality Management, Life Sciences, or Business Administration, or equivalent experience.
• Minimum of 5 years of experience in quality documentation systems, preferably in a regulated industry like healthcare or medical devices.
• Strong knowledge of FDA regulations, ISO standards, and other relevant quality management systems.
• Proficiency in document management software such as MasterControl, Documentum, or similar tools.
• Excellent organizational skills with attention to detail and the ability to manage multiple priorities.
• Effective communication skills, both written and verbal, for collaborating with cross-functional teams.
• Certification in Quality Management (e.g., ASQ CQA) is preferred.

• Competitive monthly salary range tailored to experience and location.
• Comprehensive health, dental, and vision insurance coverage.
• Generous paid time off, including vacation, sick days, and holidays.
• 401(k) retirement savings plan with company matching contributions.
• Professional development opportunities, including training and certification reimbursements.
• Flexible remote work options to support work-life balance.
• Employee wellness programs and access to fitness resources.