Remote Quality Management Jobs in Central London

1 to 4 of 4 Quality Management Jobs in Central London with Remote Work Options

Director, Global Development Quality Assurance (GDQA) - Remote

City Of London, England, United Kingdom
Hybrid / WFH Options
Proclinical Staffing
Proclinical is seeking a dedicated individual for a Director of Quality Assurance position. This role is integral to our mission of developing solutions for some of the most crucial scientific challenges of our age. The successful candidate will be a key player in our team, driving risk-based approaches … s lives. Responsibilities: Drive risk-based approach to solve complex business problems. Provide expert input to functional teams in areas such as Biostats, Data management, Clinical Trial Supply and Logistics, IRT, Pre-clinical, CMC, Clinical Pharmacology, Translational Sciences, Medical Affairs, Commercial, Regulatory Affairs and Companion Diagnostics. Drive change initiatives … in area of expertise in partnership with functional groups. Contribute to organisational quality and compliance reporting requirements. Prepare and deliver clear, informative and timely reports for service management. Lead and support the development of management reporting on quality key performance indicators. Establish and maintain regular structured interactions more »
Posted:

(Senior) Director - Clinical Technology Process & Compliance

City of London, London, United Kingdom
Hybrid / WFH Options
Hays
Major responsibilities will include a mix of (but aren't limited to): Establish the implementation roadmap for all clinical technologies that enable clinical trial management and data collection mechanisms Develop, manage and implement processes for clinical technology adoption and management, eg software solutions Drive new technology solutions for … site visits, clinical monitoring, risk management and provide clinical operations colleagues with innovative ways to make a broader impact on the lives of the patients in our studies Oversee/manage projects to integrate and implement new technologies within clinical data capture or similar Manage the creation of new … and optimisation of existing - quality management processes Liaise with colleagues, eg within IT, Clinical Operations, Biometrics, QA & Regulatory Affairs, to ensure clinical trial activities are properly integrated/aligned to protocols Manage, implement, and develop solutions in site start-up, study recruitment/conduct, and data capture processes more »
Employment Type: Permanent, Work From Home
Posted:

EMEA QSHE Lead

City of London, London, United Kingdom
Hybrid / WFH Options
Connect With Ltd
QSHE Lead - UK OR Europe, REMOTE - to £85k plus car allowance, bonus and benefits. A superb opportunity to join one of the best Facility Management companies in Europe. This is a replacement role for someone who has been promoted internally. We need someone who has experience working in a … role is based from home and will involve some travel. We require someone who has worked either for a Pharmaceutical company or a Facilities management company on site at a Pharma client. This role is focusing on the quality side of things and you will have a background … CAPA. Three direct reports 30% travel Client is a large pharmaceutical/life science company. Job purpose Provide oversight and regional strategic leadership across quality, safety, health, environment, risk management and business continuity throughout the EMEA contract. Work with other regional and global QSHE teams, subject matter experts more »
Employment Type: Permanent, Work From Home
Salary: £85,000
Posted:

Senior GCP Quality Auditor - Fully remote based in UK

City Of London, England, United Kingdom
Hybrid / WFH Options
Proclinical Staffing
Proclinical is seeking a dedicated and experienced Senior GCP Quality Auditor. This role is an integral part of the growing global team, contributing to the development and enhancement of audit strategy. The successful candidate will be responsible for conducting and managing audit activities in line with regulatory requirements and … non-routine audits according to the approved schedule and timelines. Produce audit reports and approve CAPA plans within internal timelines. Update the electronic audit quality systems as per relevant timelines. Organise and manage approximately 70% audit travel per year, following company policies. Conduct peer review of audit reports for … both internal and external auditors. Collaborate with the Head of GQA and the audit team to enhance the audit quality management system, actively participating in process improvements including QMS documentation updates. Maintain current awareness of the regulatory and pharmaceutical industry environment, influencing internal Business Partners and stakeholders on more »
Posted:
Quality Management
Central London
10th Percentile
£39,500
25th Percentile
£68,000
Median
£85,000
75th Percentile
£92,188
90th Percentile
£106,250