We're aware of a global phishing scam impersonating employees via email, WhatsApp, and Telegram, but no PageGroup systems have been breached. Find out how to protect yourself
Browse our jobs and apply for your next role.
Reach out to us or discover some great insights that could help you fill your next vacancy.
PageGroup changes lives for people through creating opportunity to reach potential.
We find the best talent for our clients and match candidates to their ideal jobs.
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.
Fantastic opportunity to join a dynamic team launching innovative technology within the medical technology sector.
The role will involve leading internal research projects aimed at expanding the drug pipeline, exclusively looking at neurodegenerative disease. You would also be supervising and coordinating activities for student / internship placements.
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.
Lead an international business in wholesale and distribution of veterinary pharmaceuticals, overseeing distribution and operations. Drive strategic growth, manage a talented team, and ensure financial success.
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.
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.
You will provide scientific expertise and technical leadership throughout the product development cycle, leading the team to ensure products are delivered on time and within specification.
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.
As a QA Auditor within the QA team you will plan and conduct audits of processes, systems, facilities, studies and documents to ensure compliance with GCP. You will play a vital role in ensuring general compliance and effectiveness of the CRO.
Create a job alert to receive Healthcare Pharmaceutical Life Sciences jobs via email the minute they become available.
Submit your CV to register with us and we will contact you if a suitable role becomes available.