MMS in Manchester is seeking an experienced GCP Auditor to safeguard trial data integrity and regulatory compliance across UK/EU audits. You will plan, conduct, and document audits of clinical sites and vendors, ensuring adherence to 21 CFR Part 11, FDA, and GxP requirements.
Join a data-focused CRO recognized for a great culture and collaborative teams. Travel up to 30% within the UK/EU, and contribute to CAPA resolutions and process improvements while working with multidisciplinary colleagues.
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Senior GCP Compliance & Audit Specialist in Manchester 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.
