MMS is a data-focused CRO seeking a Quality Auditor with strong GCP expertise to independently plan, conduct, and document audits across clinical trial sites and vendors. You will develop CAPA plans and ensure compliance with 21 CFR Part 11, FDA, and GxP requirements, while traveling up to 30% within the UK/EU.
The role requires a college degree or equivalent experience, excellent communication, and a proactive approach to problem solving in a regulated environment.
#J-18808-Ljbffr
Senior GCP Audit & Quality Compliance Lead (Global) employer: MMS
At MMS, we are dedicated to creating a workplace where your expertise as a Principal Biostatistician is valued and nurtured. Our award-winning culture promotes collaboration and innovation, ensuring that you have the support and resources needed to excel in your role while contributing to meaningful projects in the clinical research field. With a strong focus on employee growth and a commitment to maintaining an inclusive environment, MMS stands out as an exceptional employer in the UK.
