BD (Becton, Dickinson and Company) Quality Systems Specialist in Le Pont, France

Job Description Summary

As the Quality System Specialist, you are responsible for ensuring the quality system is functioning adequately for Pont de Claix Campus and supporting the quality system across all PS sites (Mexico, UK, US etc).

Job Description

The Difference of One

We are currently recruiting an experienced Quality System Specialist to join our Worldwide Systems Quality department in Le Pont de Claix (Grenoble).

You are the one who can make the difference. Join us and be a crucial part of advancing the world of health!

Quality System Specialist

As a Quality System Specialist, you will be responsible for ensuring that the quality system is functioning adequately for Pont de Claix Campus but also supporting the quality system across worldwide sites (Mexico, UK, US, etc). You will be cooperating closely with your Manager in supporting the internal and external audits and ensuring the quality system is updated to continually meet regulatory requirements as well as internal needs. You will act as point of contact for supporting questions from Customers and external Auditors related to quality systems and regulations.

Main responsibilities

  • Leading auditor for internal audits and helping with solutions;

  • Supporting closure of audit non-conformances across all Pharm Systems sites;

  • Coordinates and/or hosts external audits (customer, government, etc.);

  • Trend internal and external audit findings;

  • Updating quality systems procedures for on-going compliance and supporting efficient & streamline processes;

  • Incorporating risk-management into the quality system;

  • Stay up-to-date on industry best practices and regulations to support an effective quality system;

About you

To deliver the results that we are looking for, you are graduated in Engineering or similar scientific discipline and you have minimum of 3 years of experience in a regulated industry. You have at least a basic knowledge of regulations, preferably those of medical devices (such as ISO13485, 93/42/EEC, 21CFR820) or pharmaceutical products (Eur GMP, 21CFR210/211). You have some knowledge of technical writing and writing for complaints and you know some technical principles & tools (such e.g. statistical process methods and application, measurement systems analysis, basic quality tools: pareto, box plots, histograms, etc.).

Additionally, you are well organized and open-minded person with exceptional communication skills. You are able to work autonomously in a busy, multicultural environment. Finally, you speak English fluently.

If this describes you and your career aspirations, then please click on the APPLY button.

Interested in a career with BD, but this position doesn’t fit your skills and experience? Join our external EMEA Talent Community here:

Primary Work Location

FRA Le Pont-de-Claix Cedex

Additional Locations

Work Shift

BD is a leading global medical technology company that creates medical technology, devices and laboratory equipment for a variety of needs across the healthcare continuum. At BD, we are looking for candidates who possess passion, innovative solutions and a commitment to our one mission of improving access to groundbreaking medical and biotechnology services for people near and far, delivering state-of-the-art technology and cutting-edge research in the battle to fight and cure infectious diseases. With a global reach that extends across 50 countries worldwide, our network of professionals collaborates on effective measures to deliver enhanced patient quality such as lower health care delivery costs, improved health care and safety, and expanded health care for all. Join our company and see how you can become a part of one global mission to make a difference in human health.