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Managing a team of Analysts and Senior Analysts, you shall enhance laboratory practices and promote a culture which is consistent with cGMP, cGLP and Health & Safety within a pharmaceutical laboratory environment.Responsible for leading the Quality Control laboratory shift resources to achieve the required organisational throughput in a compliant and effective manner.
The QA and Regulatory Affairs Manager will play a fundamental role in maintaining continued regulatory compliance with standards andmedical device regulations. The ideal candidate will join a dynamic team launching innovative technology.
The Senior Director, Regulatory Affairs provides support to the Regulatory Affairs team across a range of projects as needed to support the group's activities, and works with the Vice President, Regulatory Affairs, for oversight of the team.
We are seeking an EU Business Development Director to expand client relationships and introduce high-quality preclinical research products and services. The ideal candidate will have a life sciences background, strong sales skills, and the ability to travel within the EU and internationally.
We are seeking a Managing Director to lead a medical device manufacturing site, ensuring the delivery of high-quality, regulated products to the health care market. The role involves overseeing all functions, including production, quality, supply chain, and engineering, and commercial, while driving strategic initiatives and compliance with industry standards.
As a Project Manager, you will play a vital role in getting medicines to patients who have exhausted all viable options. You will be responsible for the setup, implementation, and management of individual Expanded Access Programs.
An exciting opportunity has arisen for a Regulatory Affairs Compliance Specialist to ensure product compliance within a leading beauty-tech manufacturer. The successful candidate will focus on ensuring compliance of the beauty tech devices with the EU MDR requirements, maintaining regulatory approvals, and supporting the company's regulatory strategy in the EU.
The Client Project and Resource Manager key roles and responsibilities encompass client project initiation through to close including delegating tasks, monitoring progress, budgeting, ensuring coordination among team members and collaboration.
This is an exciting time to join this client business, as they continue on their expansion. This role has the opportunity to become trainee RP, and so is a great chance for someone looking to develop.
As the main Quality representative in Switzerland, you will form part of the EU quality team. As this business seeks to expand its portfolio of products in EU, you will be helping shape the QMS and Quality Processes, as well as serving as FvP on the wholesale and import licenses.
As the Head of Laboratory Operations you will ensure smooth day-to-day running of technical and sample operations for the business spanning scientific development activities and lab operations.
Are you a life science graduate? Or are you a healthcare professional with similar experience?
Working in R&D as a Scientist you will be supporting the team with advancing the portfolio from ideation to commercialisation. This is a lab-based role where you will be developing, optimising and executing a range of electrochemical immunoassays.
This is a fantastic opportunity to lead the R&D and PD teams in development of novel biosensing technology. You will provide technical leadership as an SME and guide strategy to successfully deliver new products.
This role will take full ownership of site quality, leading a small team of QA and QC staff. The main responsibilities will be ensuring site GMP compliance, as well as being primary point of contact for customer and regulatory authorities.
We are seeking a Senior RAQA Consultant with significant experience in Regulatory Affairs/Quality within SaMD/AIaMD. This role will work with a portfolio of medical device manufacturers so the successful candidate will be working with a varied portfolio of devices and stages.
This role will take full ownership of site quality. The client has excellent resource in the team, and we are looking for a strong leader to take strategically use resources available to drive excellent quality culture.
The Head of RAQA will be a pivotal figure, steering the Regulatory Affairs and Quality Assurance department within a IVD medical device manufacturer start up. This individual will be responsible for ensuring the company meets industry standards and regulations.
As a Scientist - Assay Development you will be supporting a number of allocated clinical trials utilising your virology expertise to develop, optimise and validate a range of assays and related techniques.
You will supervise the successful transfer of manufacturing processes from R&D to Manufacturing.You will be responsible for optimising the performance of manufacturing systems.
The Managing Director will lead a Midlands-based medical device company, responsible for driving strategic growth, overseeing financial and operational management, and ensuring regulatory compliance. This is a hands-on leadership role, offering the opportunity to shape the future of a growing business with a global presence in the healthcare sector.
The QP/RP will be responsible for ensuring that quality processes and systems are compliant with the clients policies and GMP/GDP requirements. As QP you will ensure timely batch review of products to meet demand, alongside various other QMS, Risk Management, Training and RP Duties.
This role has full oversight of EMEA Operational Quality, leading the full EMEA Quality team and ensuring continious improvement across compliance and personnel. The succesful applicant will form a key part of the senior leadership team, and will be expected to deliver against organisational goals with regards Quality Operations, and the global Quality network.
The Quality Assurance Manager / RP will be crucial in managing and improving the quality assurance systems in a leading life sciences company based in Dublin. This role involves ensuring compliance across the Quality function and leading a team to achieve excellence in quality operations.
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