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As a Senior Research Scientist in the clinical trial space, you will be leading the analytical stage of clinical trials and acting as a technical Subject Matter Expert (SME) in the scientific discipline.
Dublin based, permanent role. As Head of Quality, this role will be based around establishing and building the Quality function and establishing the first Quality presence for their new warehousing site.
As a Clinical Research Associate, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs and medical devices experts to identify, select, initiate and close-out investigational sites for pre and post market studies, ensuring adherence to applicable regulations and principles of ICH-GCP.
As a Senior Proposal Manager you will be responsible for managing all aspects of proposals, monitoring and overseeing the scope of work and budgeting process to generate accurate and timely proposals.
Manage and coordinate all laboratory operations, including sample processing, data analysis, and quality control procedures. Oversee the allocation of resources, ensuring optimal utilization of equipment, supplies, and personnel.
As an SDS Specialist / Hazard Comms professional you will primarily focus on working within the EU market to provide technical scientific input into SDS generation / updates.
Leading development and validation activities with predominant focus on LCMS / triple quad MS, designing and developing quantitative bioanalytical methods in support of PK and PD projects
You will be planning and managing patient-reported outcome & clinical-outcome assessment development and validation projects for drug development projects, delivering high quality results and establishing strong collaborator-relationships.
Principal Scientist in Polymer Development leading on the development of water soluble barriers and coatings for absorbent hygiene products.
Principal scientist in Drug Delivery - offer leadership on the development of drug delivery systems for the oral administration of small molecules and biologics, mentor junior members of staff and engage with external stakeholders.
Searching for a highly motivated Senior Biomedical scientist with experience in the Genomics space to become part of a friendly and sociable referrals team.
Searching for a highly motivated Biomedical scientist with experience in the Histology space to become part of a friendly and sociable team.
Searching for a highly motivated Biomedical scientist with experience in the Haematology space to become part of a friendly and sociable team.
As a Principal Scientist based in the Leeds area you will oversee the creation of new product specifications, develop test methods to transfer into manufacturing / QC, and support with investigations and validations as required.
Become an integral part of a growing orgainsation.Play a key role in delivering life changing health care services.
My client is seeking a Sales Director to lead sales of CMO services/ API products to Pharmaceutical organisations by pursuing new business opportunities, establishing relationships with key partners, and developing and executing strategies to drive revenue growth in the UK. This is an individual contributor position but will work closely with the senior leadership team to implement business plans, evaluate potential partnerships and negotiate complex deals.
The Integrity & Compliance Manager/Associate Director will be responsible for supporting, managing and enhancing Most of World (MoW) implementation of the Global Integrity & Compliance Program (HCC focus).Establishing clear policies and offering pragmatic, solutions-orientated guidance and program support to the AUA Integrity & Compliance Officer.
Providing support within the regulatory function maintaining and expanding the specified product registrations within UK and EU.
The purpose of this role is to make sure that the labelling is updated and compliant and meets the necessary trademark deadlines.
As a part of the regulatory team you will be responsible for obtaining and maintaining generic and branded marketing authorisations for designated EU and non-EU territories (through internal and Third Party workstreams) to ensure on-time launches, continued supply and the compliance of all products. This roll will also provide the opportunity to develop management skills within the team.
As a part of the regulatory team you will provide UK national support for new product MR/DC or CP submissions managed by CRA teams and provide support to other UKRA team members as required and assist other UKRA team members to produce documentation and submissions.
Responsible for life cycle management relating to variation submissions, renewals, labelling updates and preparing dossiers to meet national submission requirements. You will also be maintaining national aspects of Global Regulatory Systems.
Leading projects with small to medium complexity to develop and commercialise new products.
You will be developing regulatory strategies from development through to the post approval phase whilst obtaining regulatory approvals and registrations for innovative medicinal products within the EU.
To perform Regulatory tasks as required to ensure regulatory compliance
Oversee all aspects of the company's quality management system, current product regulatory compliance, and participate in medical device development projects contributing to the quality assurance and regulatory affairs deliverables as required.
The Regulatory Affairs Director will report to the Global Head of Regulatory at Sinclair and will support the innovation, international and patient- centric strategies enabling simultaneous global access to our products.
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