Quality Specialist

  • Career level: Direct Entry
  • Employment: Fulltime, permanent
  • Start: immediately
  • Location: Enfield, CT (US)
  • Job-ID: R3170

Would you like to work for a company who has made it its mission to make a contribution to improving human living conditions? With around 4,500 employees worldwide Eppendorf is a leading Life Sciences company. We develop and distribute devices, consumables and services for use in laboratories worldwide. Our daily work is characterized by our principle: Collaborate on new ideas. You would like to take responsibility and help to make a difference in an experienced international company? Exciting tasks combined with a positive and affirmative working environment await you at Eppendorf. You are also motivated by technical challenges? Then apply now!

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Your challenges

  • Organize and reviews the specified quality validation documents for bioprocess equipment (BPE) pressure vessel systems (pressure vessel documentation, welding records, calibration records, and all part certifications).
  • Provide assistance for document control and management, including Quality Management system documents and records.
  • Support administration of the gage calibration and maintenance program for the manufacturing and lab areas.
  • Conduct final product inspections for BPE products.
  • Conduct internal audits, as required.
  • Work closely with the Quality group, Engineering, Manufacturing, Planning and Purchasing to identify product issues and determine a course of action.
  • Follows ISO 9001 and 13485 policies and procedures in the performance of the responsibilities outlines in the job description.
  • Initiates and/or making suggestions to improve working processes or productivity, etc.
  • Performs other QA and related activities as assigned Assists Quality Management in the creation, development and revision of inspection documentation

Your expertise

  • HS Diploma or GED, but 2-year Associate degree (A.A.) in Engineering or Science preferred.
  • Three to five years’ experience in incoming inspection, quality control or a similar job experience.
  • Experience within a cGMP, ISO 13485 (Medical Devices) or other regulated manufacturing environment is preferred.

Your benefits at Eppendorf

  • Competitive total rewards package including health, financial, and education benefits
  • Innovative and Collaborative corporate culture
  • Contribute to improving the human living condition
  • Direct impact on business

Please note that we can only consider applications that are submitted online via our application management tool.

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