Job ID R-400448 Date posted 11/02/2021

Be part of something bigger at BD. Here, you’ll join a driven, agile engineering team working in a startup-like environment that has the backing and resources of a Fortune 500 company. In engineering, you could be involved in everything from operations, production and construction to information technology and maintenance environments, all while analyzing and developing solutions to further our engineering capabilities. You’ll use your talent and track record of solving complex problems to achieve one singular goal: advancing the world of health™. At BD, you can make a true difference of one.

  • Job Type:
    Full-Time
  • Job Level:
    Entry to Senior
  • Travel:
    Varies
  • Salary:
    Competitive
  • Glassdoor Reviews and Company Rating

Responsibilities

Job Description Summary

The Manufacturing Engineer I - Engineering Change Coordinator will be a key contributor within the Manufacturing Engineering team in managing engineering change orders, including facilitating the impact assessment and communication to affected functions, collecting and/or creating engineering deliverables, and participating in change implementation into Production and other customers, internal and external.

Job Description

The Manufacturing Engineer I – Engineering Change Coordinator will have the opportunity to learn complex diagnostic instrumentation in a top medical device manufacturing company by supporting the Manufacturing Engineering staff in engineering change order initiation, management and implementation.

The ME I will be deeply engaged in creating and maintaining product structures, master data and manufacturing documentation, while ensuring shop-floor control, quality system compliance and ERP data integrity, and over-all Production readiness during essential product and process changes.

The ME I will work with other functional groups, such as Quality, Regulatory Affairs, Research & Development, Service, Procurement, Production Planning, Master Data and Document Control and other associates supporting new product development or sustaining engineering projects.

In the process, the ME I will earn a brilliant experience in his/her career by becoming familiar with complex flow cytometry instruments along with the operational and technical activities in manufacturing and sustaining these medical devices.

Duties and Responsibilities

Initiate, plan and author engineering change orders to product design, product documentation, Bills of Materials, manufacturing/test/packaging procedures, process routings, tooling, compliance (EMC, safety, laser safety, ROHS, UDI etc), suppliers and other items in a controlled manufacturing environment.

Prepare, create, and maintain various types of SAP data objects. Redline bills of materials, assembly, test, and specification documents. Update other technical and compliance documents.

Coordinate with various functions for change review and impact analysis, ensuring cross-functional requirements are identified and understood for affected items, personnel and processes .

Work closely with multiple associates throughout the duration of projects, in reviewing, updating and submitting information for the preparation of various documents and engineering change deliverables.

Ensure accuracy of information within controlled documents.

Follow proper document formats, material and description nomenclature, and correct SAP data types per company standards.

Communicate and collaborate with change reviewers/contributors, signatories, and Document Control Specialists. Track and update the status of change orders.

Participate in manufacturing floor readiness during implementation of changes, including material changeovers, material disposition (quarantine, scrap or rework), tool installation, Kanban setup, and personnel training. 

Communicate changes to external suppliers to assist in timely implementation at their sites.

Ensure all ECO changes occur in a timely manner and perform the necessary follow-up to prevent any conflicts or delays to business goals.

Keep abreast of the basic requirements for regulatory compliance in own area of work and comply with those requirements. Participate as required in training on regulatory issues affecting own area of work. Bring regulatory compliance questions/issues to the attention of management.

Capable of generating and/or revising Manufacturing specifications, procedures, and other technical documents for medical device products

Minimum Requirements:

  • Require a BS degree: ME, EE, IE, IT or equivalent education and experience
  • 0 - 3 years’ experience in product documentation and manufacturing operations
  • Work in a med device environment required
  • Excellent written and verbal communication skills, must have good interpersonal skills and the ability work in a team environment
  • Excellent writing skills to author Engineering Change Orders with change descriptions, reasons, justifications, and supporting information
  • Experience in developing manufacturing assembly, test procedures and product structures
  • Must be proficient in the use of personal computers and Microsoft Office (Excel, Word, Visio, and MS Project (PowerPoint)) and Adobe products
  • Must be able to understand engineering drawings, Bills of Materials, and operational procedures
  • Ability to assess and resolve multiple high visibility problems timely
  • Familiarity with ISO 9001 and 13485 standards

Desirable Qualifications

  • Broad experience supporting complex medical devices and many of the following commodities or supplier types: lasers, optical components, fluidic systems, machined parts, sheet metal, cables, PCA’s, plastics, power systems, product packaging, turnkey subcontractors, hardware, labeling
  • Proficient with Pro-E, AutoCAD, or SolidWorks
  • Experience leading meetings both in-person and virtual
  • Daily working knowledge of SAP product documentation system and lifecycle management (engineering changes)
  • Experience presenting to large and diverse types of audiences
  • Effective organizational, planning and prioritization skills

Employment at BD is contingent upon the Company’s receipt of sufficient proof that you are or will be fully vaccinated against COVID-19.  Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

“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.”

Primary Work Location

USA CA - San Jose

Additional Locations

Work Shift

NA (United States of America)
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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.

As a new employee what I like most about BD are the many learning and professional developmental opportunities for growth offered. It is good to know that there are so many resources to choose from.


Zakiyyah Walker
Staff Engineer

Since joining BD, I really have liked the people I work with on a daily basis and the collaboration towards common goals.


Michael Carrano
Senior Program Manager

BD is full of passionate, loyal, and driven people that have a common goal of advancing healthcare without sacrificing quality or service.


Justyna Zielinska
Project Manager

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