Director of GxP Compliance - England

The immense cost and complexity of GxP validation has locked the Life Sciences industry out of the modern software and AI revolution. · We are building a product at the intersection of three profoundly difficult domains: GxP-compliant systems, AI-native workflows, · and world-cla ...

We're seeking a Sap & it quality risk & compliance manager to lead and support compliance across application support and delivery functions ensuring adherence to governance security documentation standards. · Provide leadership to ensure IT services solutions meet quality complia ...

We are seeking an experienced Head of Warehousing to lead pharmaceutical warehousing operations at a large, · regulated distribution site in Warrington.This senior leadership role holds full accountability for operational performance, · regulatory compliance, people leadership, a ...

We're seeking a SAP and IT Quality, Risk and Compliance Manager to lead and support compliance across application support and delivery functions. · ...

We are seeking an experienced SAP QM Consultant with strong domain knowledge in pharmaceutical industry. The ideal candidate should have hands-on expertise in SAP QM modules and deep understanding of GMP,GxP,FDA regulations,and pharma manufacturing processes. · ...

An SAP QM Consultant specializing in the pharmaceutical sector designs, configures, implements, · and validates the SAP QM module tailored to GMP/GxP-regulated environments. · Ensure GxP/GMP compliance throughout SAP QM processes. · Translate pharma quality processes (inspection, ...

We are seeking an experienced Senior Regulatory Information Management (RIM) Specialist with deep expertise in Ennov RIM to support global regulatory operations for pharmaceutical, biotechnology, or life sciences organizations. · Act as a subject matter expert (SME) for Ennov RIM ...

This is a full-time on-site role based in London for a QA (Sr.) Specialist.The QA (Sr.) Specialist will be responsible for overseeing quality assurance processes, conducting quality audits, ensuring compliance with Good Manufacturing Practice (GMP), maintaining quality control me ...

The job involves providing ongoing engineering validation support to MeiraGTx sites, ensuring compliance with EU and FDA regulations. The successful candidate will have a degree in Human Health or Sciences and at least 5 years of experience in Engineering Validation department. T ...

Veeva Consultant required with SAP experience on a contract basis working remotely for our client based in London. · ...

This is a full-time on-site role based in London for a QA (Sr.) Specialist. · The QA (Sr.) Specialist will be responsible for overseeing quality assurance processes, conducting quality audits, ensuring compliance with Good Manufacturing Practice (GMP), maintaining quality control ...

We are hiring a Validation Lead to drive regulatory compliance and Computer System Validation (CSV) excellence in our SAP-centered validation offering. · ...

SAP QM Consultant specializing in the pharmaceutical sector designs, configures, implements and validates the SAP QM module tailored to GMP/GxP-regulated environments. · ...

We are currently searching for a Senior Compliance & Quality Assurance Consultant – ATMP – Qualified Person to join the team in the UK to support a range of clients primarily operating in the ATMP/Cell and Gene therapy area. · The Senior Compliance & Quality Assurance Consultant ...

Wearelookingfora highlyskilledSalesforceVeevaFunctionalleadojointheirteamonapermanentbasisinLondon.ThisroleisidealforaSalesforceprofessionalwithdeepVeevaexperience,strongfunctionalleadershipskills,andapassionfordeliveringimpactfuldigitaltransformationwithinLifeSciences. · ...

This is a full-time on-site role based in London for a QA (Sr.) Specialist. The QA (Sr.) Specialist will be responsible for overseeing quality assurance processes, conducting quality audits, ensuring compliance with Good Manufacturing Practice (GMP), maintaining quality control m ...

An SAP QM Consultant specializing in the pharmaceutical sector designs, configures, implements and validates the SAP QM module tailored to GMP/GxP-regulated environments. · ...

To support the maintenance, enhancement, and integration of Richmonds software systems, with a focus on reliability, security, and compliance. · The Software Engineer will contribute to the implementation of off-the-shelf software,assist in validation activities, · and provide re ...

Associate Director, Tech QA will work with IQVIA divisions including its wholly owned subsidiary and laboratory division, IQVIA Laboratories . · ...

The Associate Director of Tech Quality Assurance will work with IQVIA divisions including its wholly owned subsidiary and laboratory division. · Organize Clinical Trial Laboratory Technology Systems Audit activities in IQVIA globally. · Evaluate audit findings and prepare reports ...

Job summary · An international company in the pharmaceutical industry is looking for a Senior ERP Analyst with good knowledge of the pharmaceutical / medical sector to join their team. · Responsibilities:define requirements and translate to system configuration in the Oracle ERP ...