• Job Description

  Req#: R1246725

  Wondering what’s within Beckman Coulter Diagnostics? Take a closer look.

  At first glance, you’ll see that for more than 80 years we’ve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, supported, and always be yourself. We’re building a culture that celebrates the backgrounds, experiences, and perspectives of all our associates. Look again and you’ll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful.

  Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges.

  The Quality Assurance Scientist for Beckman Coulter Diagnostics at the Kentucky Facility is responsible for performing Finished Product evaluation of batch records and Incoming Inspection/Finished Product Release. The Job requires Strong Documentation management skills that focus on Quality with Key Performance Indicators and timelines.

  This position is part of the Product Release Quality Control Department located in Florence, Kentucky and will be on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time!

  You will be a part of the Quality Control team and report to the Quality Control Manager at the Kentucky Manufacturing Facility and will be responsible for Quality Batch Record reviews and Incoming/Finished Product Testing. If you thrive in a fast-paced environment with multiple supporting roles and want to work to build a world-class supply chain organization—read on.

  In this role, you will have the opportunity to:

  • Perform incoming inspection of components as needed working with daily output requirements.
  • Documentation Management
  • Drive process improvements and change by using/developing DBS skills.
  • Perform Evaluation of Batch Records with a focus on regulatory compliance against GDP and FDA regulations.
  • Release finished product for customer use in a fast-paced environment.

  The essential requirements of the job include:

  • Bachelor’s degree with 2+ years of experience or Master’s degree with 0+ years of experience.
  • Demonstrated experience working with highly detailed information including document management-related activities.
  • Proficiency with Microsoft Excel, Word, Outlook
  • Experience working in a highly regulated environment driven by ISO QMS standards.
  • Exposure to QMS

  It would be a plus if you also possess previous experience in:

  • Working in an FDA Regulated Environment with a focus on documentation requirements
  • Experience working within a global organization
  • Audit experience
  • Previous experience working with continuous improvement

  #LI-MR1

  3-5-7 model for Job Requirements

  P Level position requires 5

  1. Education- 4-year degree, preferably in the science field

  2. Years of Experience- 3-5 years of functional experience

  3. Detail Oriented with focus on Documentation management.

  4. Thrive under a fast-paced environment, requiring daily outputs.

  5. Ability to multitask to ensure customer needs are continually met.

  When you join us, you’ll also be joining Danaher’s global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.

  Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
  
  The EEO posters are available here .
  
  We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation.
  
  If you’ve ever wondered what’s within you, there’s no better time to find out.

• About the company

  Danaher Corporation is an American globally diversified conglomerate with its headquarters in Washington, DC.

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