Quality Management and Regulatory Affairs, Manager

  • Career level: Direct Entry
  • Employment: Fulltime, permanent
  • Start: immediately
  • Location: Enfield, CT (US)
  • Job-ID: R4710

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

  • Manages the Quality Management system and Regulatory compliance for the Americas market region related to Global Supply chain functions including warehouse, logistics and customer support functions.
  • Supports and maintains with Global Quality and site management to assure Eppendorf compliance to quality standards and regulatory requirements.
  • Drives process and continuous improvements based on the collection and analysis of data, business and customer requirements, together with regional process experts & owners
  • Contact point for feedback as well as process and normative guidance
  • Plays a central change management role in the deployment of processes and software tools
  • Leads projects for process optimization and implementing related methodologies
  • Define and maintain business processes along the Eppendorf value chain as part of the corporate quality management department
  • Build and maintain a network of country and regional process experts & owners
  • Achieves process execution by training, guiding and directing key and end users on processes, responsibilities and tools
  • Define Key Performance Indicators and support their implementation in software tools and manage reporting

Your expertise

  • **Employment at Eppendorf requires vaccination against Covid-19, or, an approved accommodation due to a qualified exemption**
  • Bachelor’s degree required.
  • Experience in the Life Science or Medical Device industry is preferred.
  • Strong collaboration skills, the ability to influence without direct authority, and the ability to work effectively cross-functionally
  • At least 5 years professional experience in the field of process management, quality management (9001, 13485) or project management

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.

Apply now