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CooperSurgical is a leading fertility and womens healthcare company dedicated to putting time on the side of women babies and families at the healthcare moments that matter most in life. As a division of CooperCompanies were driven by a unified purpose to enable patients to experience lifes beautiful moments. Guided by our shared values dedicated innovative friendly partners and do the right thing our offerings support patients throughout their lifetimes from contraception to fertility and birth solutions to womens and family care and beyond. We currently offer over 600 clinically relevant medical devices to healthcare providers including testing and treatment options as well as an innovative suite of assisted reproductive technology and genomic testing solutions. Learn more at.
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At CooperSurgical we are currently looking to recruit a Quality Manager-for our Distribution Center (DC). In this role there will be one direct report and much cross- functional collaboration and stakeholder management withlocal regional and corporate CSI organizations.
You will be part of the CooperSurgical Regional Quality team with direct reference to the Director of Quality Assurance OUS manufacturing distribution and service. The role is placed in Venlo Netherland and is onsite.
Applicants must be eligible to work in Netherland and travel freely in EU UK and APAC.
Position
As Quality Manager you will play a critical role in ensuring regulatory compliance implementation continuous improvements and consistent performance of CSI quality management system requirements at Venlo DC site.
In this role you will be the Quality subject matter expert of the end-to-end finished goods supply chain enabling thedistribution quality standards and regulatory compliance for the EMEA and part of APAC regions.
The Quality manager is responsible for providing quality oversight for area specific change controls deviations and CAPAs and participate in and reviewing investigations.
Its essential to ensuring that products received/stored/labeled/shipped from Venlo DC meet the required quality standards and customers expectations in compliance with the requirements of the European (MDR) Medical Device Regulation 2017 / 745 on medical devices European In Vitro Diagnostic Regulation (IVDR) 2017/ 746 ISO 13485 standard including FDA CFR Part 820 Quality System Regulation.
As CooperSurgical have satellite distribution centers in Turkey Australia /NZ and India its important to work closely with these countries and be familiar with their local regulations.
This position requires a seasoned professional with a deep understanding of GMP GSP and GDP practices excellent problem-solving skills and the ability to collaborate across cross-functional teams.
You thrive in a dynamic environment and are comfortable juggling several complex tasks while keeping an eye on the details. You will work closely together with the Quality and Regulatory teams and relevant stakeholders globally.
Your key responsibilities
Required Experience:
Manager
Full-Time