Quality Assurance, Business Process Engineer (m / w / d)
Based in Frankfurt
Our client is a global leader (top 10 worldwide) of active medical devices at Class III and pharmaceutical drugs. They are in the middle of a global project across 54 sites in EMEA, Latin America and Asia Pacific to reduce complexity in business processes for the QM department by designing new interfaces and sub-systems for all areas of quality - design control, CAPA, Supplier Management, PMS.
There is a need for Business Process Engineer with experience within Medical Devices and Quality Management to design QM processes and translate them into the IT system as part of the worldwide SAP rollout.
The role works closely with the day-to-day business operations and translating business processes into a standardized SAP system - the IT department will do this for you. You are not expected to be an IT mastermind, and have a strong grasp on the quality aspects instead.
As the project leader, your ultimate aim (alongside quality compliance) is data integrity, transparency and efficiency in business processes for the global Quality team across 34 sites.
The skill set required for this position is experience in Medical Devices and quality processes under ISO 13485, ISO 9001 and GMP.
If designing Quality Management Processes within a Medical Device setting is your area of interest and expertise, and the chance to do that on a large global scale excites you - this will be a highly relevant opportunity that we should discuss. Please do reach out to me at Rebecca.Stevens@adaptivelifescience.com for an informal discussion.