Future Tech Jobs
Future Tech Jobs
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...
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...
This role involves managing procurement activities, supplier relationships, and quality management within a regulated pharmaceutical manufacturing environment. You will work closely with the Manufacturing, Quality, and Operations teams to ensure effective sourcing and compliance with GMP standards.
This role involves performing routine and non-routine analysis of raw materials and finished pharmaceutical products using techniques such as HPLC, GC, UV, and FTIR. The analyst will lead Out of Specification investigations, ensure compliance with GMP standards, and contribute to method development and validation. It is a site-based laboratory position requiring strong documentation, troubleshooting, and analytical skills in a regulated environment.
The Research Associate will manage inventory, prepare reagents, and run automated systems for high-throughput screening. They will collaborate with cross-functional teams to optimize workflows and adopt new technologies, contributing to the company's drug discovery platform.
This role involves operating chemical process plant and manufacturing equipment, following batch manufacturing instructions, monitoring chemical reactions, and supporting material handling and packaging activities. The position offers long-term stability and development opportunities within a safety and quality-driven manufacturing environment.
This role involves planning, coordinating, and monitoring production activities across multiple projects in a regulated medical device manufacturing environment. You will work closely with manufacturing, engineering, quality, and supply chain teams to ensure delivery targets are met and continuously improve planning processes.
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.
As a Process Technologist, you will support the production area by providing technical services, troubleshooting, and working on technical projects. You will collaborate with cross-functional teams to ensure product quality and compliance, execute process validation, and perform root cause analysis for material and processing issues.
Director, Quality Assurance (Diagnostics & Devices)Cambridge, UK (3 days on site per week)About AstraZenecaAstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases....
Leads end-to-end supply planning and execution for a designated therapy area, ensuring uninterrupted patient access to medicines. Works cross-functionally across planning, manufacturing, quality, and commercial teams to resolve supply disruptions, drive inventory optimisation, and implement continuous improvement initiatives using data analysis and planning systems. Focuses on risk mitigation, regulatory compliance, and performance monitoring within a global pharmaceutical supply chain.
Your work will change lives. Including your own.The Impact You’ll Make:Recursion is currently seeking a seasoned leader to join our team as Vice President, Real World Experience. This role will lead RWE generation across the Recursion portfolio. The role will...
The Business Development Manager will focus on driving revenue growth and expanding market share for a respected UK medical technology provider. Key responsibilities include identifying new opportunities, building relationships with NHS leadership, and executing key account strategies across the South of England.
Role: Operations ManagerSalary: £50,000-£55,000Location: NottinghamshireThe role:We are looking for an experienced Operations Manager to take responsibility for the day-to-day running of a GMP-regulated manufacturing and distribution facility.Reporting into the UK Managing Director, you will have overall responsibility for site operations,...
This role involves leading regulatory strategy for EU and US markets within a pharmaceutical CDMO, managing submissions to EMA and FDA, and overseeing regulatory documentation for complex drug products. The candidate will act as a key liaison with global regulatory agencies and lead a small team, contributing to lifecycle management and regulatory intelligence. The position requires deep expertise in centralised procedures, dossier compilation, and cross-functional collaboration in a fast-paced environment.
As a Regulatory Manager, you will lead regulatory strategy for drug-device combination products, working closely with global regulatory bodies and clients. You will manage a small team, review key documentation, and contribute to regulatory intelligence, with opportunities for career growth in a forward-thinking, innovative company.
This role involves developing and executing high-quality HTA, Value & Evidence strategies to support patient access and reimbursement for Rare Disease treatments. The Senior Manager will manage health economics and outcomes research, collaborate with cross-functional teams, and ensure a consistent evidence generation strategy across markets.
