Future Tech Jobs
Future Tech Jobs
CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...
The Director, Biostatistics, leads the full scope of statistical contribution to a clinical development program, including life cycle management. The AD provides for statistical excellence in clinical development plans, trial planning, data analysis, interpretation and reporting, and regulatory interactions and...
The Regulatory Affairs Assistant will provide administrative, operational, and compliance support to the Regulatory Affairs team, ensuring accurate data and documentation, supporting team processes, and maintaining compliance with regulatory standards. The role involves a broad range of activities, including regulatory file compilation, database management, project coordination, and administrative support to the Head of Regulatory and the team.
Cure Talent are delighted to be partnered with a global medical device organisation recognised as one of the most established and successful healthcare companies in the world. With a diverse international footprint and a strong pipeline of innovation, the business...
Regulatory Affairs Assistant – Devon – Up to £30,000 + Benefits – REF 065£25,000 pa - £30,000 pa + Company Bonus + BenefitsDevonMon – Fri40 hours p/wAn exciting opportunity has arisen to join a global manufacturing organisation that develops, manufactures,...
Evolve are partnering with a fast-growing organisation to appoint a Head of Quality Assurance & Regulatory Affairs. This is a strategic leadership role where you will drive quality and regulatory excellence, support global expansion, and work cross-functionally to ensure consistently...
This role involves leading the development of global regulatory strategies for drug development programs, managing regulatory activities, and collaborating with cross-functional teams. The position requires extensive experience in regulatory affairs, with a focus on global health authorities and regulatory submissions.
Label Strategy Manager (Devices) - EuropeLocation: Maidenhead/Remote (Hybrid working model)Contract: Temporary, full-time (7‑month maternity cover), starting July 2026Rate: Negotiable - circa. £60-70 per hourAn exciting opportunity has arisen for an experienced Label Strategy Manager (Devices) to join a European labelling...
As a Regulatory Conformance Officer, you will ensure that GSK's products meet all licensing and regulatory requirements, maintaining compliance with global market authorisations and supporting regulatory submissions. You will collaborate with multiple functions, including manufacturing, R&D, and global regulatory affairs, to deliver regulatory strategies and inspection readiness.
TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...
TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...
In this role, you will manage the end-to-end execution of clinical trial registration and results posting, ensuring Roche complies with global regulations. You will lead the accurate and timely posting of clinical trial data, manage cross-functional teams, and ensure consistency and quality in all submissions.
The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global goals and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, anticipating risks, and driving timely submissions and approvals.
Are you an experienced regulatory professional looking for your next long-term career move?I am partnering with an innovative, medical technology business to find a dedicated Regulatory Affairs Specialist to join their growing RAQA team on a permanent & 100% remote...
This role involves supporting quality, regulatory, and information security processes in a growing laboratory setting. Responsibilities include maintaining the Integrated Management System, ensuring compliance with various standards, managing controlled documentation, and assisting with audits and risk management.
My client, an innovative technology business within the medical device sector, are seeking a Quality Assurance & Regulatory Affairs Manager to join their team.Working closely with senior leadership, R&D and operations, you will play a pivotal role in bringing products...
This role involves leading the design, execution, and reporting of post-authorisation safety studies using real-world data. The candidate will collaborate with various teams to produce high-quality evidence for regulatory decisions and risk management, ensuring AstraZeneca's medicines are safe and effective.
