ZEISS Group seeks a senior Quality & Regulatory professional to lead EU QMS governance across Medical Devices, cosmetics, and related products. You will ensure compliance with EU quality frameworks and align product lifecycle activities with MDR, ISO 13485, and ISO 14971 requirements.
In this role you will drive governance, supplier quality interfaces, and post-market vigilance, while supporting audits, CAPAs, and regulatory submissions within a matrix organization.
#J-18808-Ljbffr
EU Quality & Compliance Lead: QMS, MDR & Audits in Birmingham employer: ZEISS Group
At ZEISS, we pride ourselves on being an excellent employer, offering a dynamic work environment in Cambourne that fosters innovation and collaboration. Our employees benefit from flexible working hours, a hybrid model, and clear pathways for career advancement, ensuring that you can grow alongside our globally recognised technology company. Join us to make a meaningful impact in the manufacturing supply chain while enjoying a supportive culture that values proactive and motivated individuals.
