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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Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team?
City of Edinburgh
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team?
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Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team?MMS is a…
Manchester
About MMS Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team?
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