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PageGroup changes lives for people through creating opportunity to reach potential.
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Looking for a dynamic and hands-on General Manager to lead the innovation business, aligning with their values and growth plans.Location : Open ( preference is Australia, visa support provided )
This role involves the management of finance operations in a fast-paced environment. The successful candidate will play a vital part in driving the company's financial strategy and planning.
The Finance Business Partner is a pivotal role in the Accounting and Finance Department within the Life Science industry, based in Cambridge. The role will involve strategic planning, budgeting, and forecasting.
This role as a Senior Clinical Quality Assurance Associate is crucial in maintaining and enhancing the quality standards of successful clinical trial delivery. You will be responsible for ensuring active participation in continuous quality improvement activities, working closely with Clinical Operations and other supporting areas.
This role will involve leadership of the Quality function, and its associated teams. The main areas of focus will be in driving compliance to GMP, as well as improving current processes and practices.
This role for a Senior Financial Accountant is an exciting opportunity for an individual keen to bring their expertise to the life sciences industry. The successful candidate will be responsible for leading financial operations and driving financial reporting and analysis within a thriving department.
An exciting opportunity has arisen for a diligent and motivated HR & Payroll Manager to take the helm at our Human Resources Department in the Life Science industry.
In this role, the Senior RAQA Consultant will work closely with Clients, implementing Quality Management Systems, Clinical Design Controls, and full software lifecycle process.
A part time interim position for a global business based in Stevenage. The interim candidate will support with Accounts Payable and Case Management. The role on offer will be split over 18.75 hours and can be worked flexibly across the working week.
We are seeking a meticulous and dedicated Senior Regulatory Affairs Associate with a strong background in Regulatory Affairs (Medical Devices). The successful candidate will be responsible for ensuring compliance with regulatory standards (MDD-MDR experience is essential).
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