Future Tech Jobs
Future Tech Jobs
Latest UK roles, updated daily.
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...
Two Directors of Search & Evaluation to lead strategic sourcing and evaluation of external innovation opportunities in Hematology, and Cardiovascular/Renal therapeutic areas. Embedded within each Therapeutic Area Leadership Team (TALT), these leaders will identify and advance high-potential assets from preclinical...
This role involves leading a global matrix programme team to transform incoming material testing and data management across GSK's manufacturing sites. Responsibilities include defining future-state operating models, creating global standards, and ensuring harmonised QC master data structures while partnering with various teams to implement the strategy.
This role involves leading Extractables and Leachables (E&L) assessments for biopharmaceutical manufacturing processes, container closure systems, and dosing devices. The Specialist will work with internal and external labs to ensure E&L testing is completed scientifically, compliantly, and cost-effectively, while also managing risk identification and escalation.
This role involves preparing and maintaining Environmental Risk Assessments, monitoring outsourced environmental studies, and engaging with cross-functional teams on sustainability initiatives. The position offers hands-on experience in regulatory science and environmental data interpretation, with full training and mentoring provided.
This role involves crafting and driving the global Oncology R&D strategy, integrating clinical, scientific, and commercial insights to shape portfolio priorities. You will advise senior leadership, optimize investment decisions, and collaborate across functions to deliver high-impact strategic outcomes.
The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization...
The Role:Reporting to the Director, Business Analytics & Operations Management, the Associate Director, Business Analytics & Insights, Clinical Operations will be accountable for development and implementation of analytical & financial systems & tools and processes to perform business analytics within...
Your work will change lives. Including your own.The Impact You’ll MakeAt Recursion, our mission is to industrialize and transform the development of medicines by integrating data-driven insights and advanced analytics throughout the entire development lifecycle. As Executive Director, Asset Project...
Your work will change lives. Including your own.The Impact You’ll MakeAt Recursion, we are reimagining drug discovery through a powerful synthesis of AI, automation, and deep scientific expertise. In this role, you will be the bridge between complex chemical data...
This role involves assembling high-quality medical devices in a cleanroom environment, following strict GMP standards and ISO procedures. The position offers a 4-day work week, comprehensive training, and a range of benefits including private healthcare and a company pension.
The Compliance Engineer will be responsible for planning and conducting compliance and testing for medical products, ensuring adherence to UK, USA, and EU standards. They will also maintain test equipment, write and check reports, and drive continuous improvement within R&D.
The Business Analyst will support a key programme focused on the collection, tracking, and lifecycle management of human biological samples. Responsibilities include eliciting and documenting requirements, mapping end-to-end processes, and facilitating stakeholder workshops to enhance biobanking systems and data flows.
This role involves leading a small QA team, ensuring compliance with regulatory standards, and overseeing quality systems and validation activities. Responsibilities include report writing, managing QA documentation, participating in audits, and driving continuous improvement initiatives.
As a Technical Writer, you will document and standardize internal processes for a global biopharmaceutical company, focusing on clarity and accountability. You will interview subject matter experts, maintain the 'Policy Hub', and ensure all documentation aligns with the company's vision.
