Future Tech Jobs
Future Tech Jobs
Quality & Continuous Improvement SpecialistSalary: £36,000 - £42,000 + 5% BonusThe OpportunityI'm currently working with an established engineering manufacturer that supplies specialist products to customers across a variety of industries throughout the UK and internationally.This is an excellent opportunity to...
This role involves leading the clinical operations strategy and execution across Recursion’s development portfolio, from study planning to study closeout. You will build and mentor a high-performing team, manage global trials, and ensure operational excellence in an AI-native TechBio company.
This role involves designing and delivering bespoke pharmaceutical process equipment and systems, ensuring compliance with strict regulatory standards. Responsibilities include conducting site surveys, producing detailed drawings, and collaborating with multidisciplinary teams to ensure integrated system functionality.
The Validation/Quality Assurance Specialist will plan and execute validation activities, author and maintain validation protocols, and collaborate with cross-functional teams to ensure compliance with GMP standards. The role involves maintaining validated status, supporting regulatory inspections, and contributing to the Site Validation Master Plan.
This role involves ensuring compliance with Good Distribution Practise (GDP), ISO 9001, and ISO 13485 standards through quality assurance activities such as managing deviations, change controls, audits, and supplier verifications. The Quality Officer will support the Quality Management System, conduct investigations, review documentation, and prepare for regulatory inspections. They will work closely with internal teams and external stakeholders to maintain product quality and process safety in a regulated environment.
Engineering technician - mechanical, mechatronics or electricalAdvanced Biomedical Technology | West London full time on siteThis is a rare opportunity to join a growing company at the forefront of advanced biomedical engineering.Are you an ONC/HNC (or higher) qualified technician/engineer with...
This role leads statistical programming efforts across global clinical trials, managing teams and driving innovation in data analysis and visualization. The individual will shape programming strategy, ensure audit readiness, and collaborate with cross-functional teams to deliver high-quality statistical outputs. Emphasis is placed on adopting modern tools like R, Shiny, and Git for reproducible, standardized workflows in drug development.
The Global Labelling Director, Content (Immunology) will lead the development and delivery of high-quality global labelling strategies for innovative medicines. Key responsibilities include shaping labelling content, ensuring regulatory compliance, and collaborating with cross-functional teams to support successful product submissions and patient safety.
This role involves managing regulatory submissions and product lifecycle compliance for pharmaceutical products, with a focus on packaging, labelling, and interactions with the MHRA. The candidate will coordinate eCTD submissions, support variations, and ensure change control processes are followed across cross-functional teams. It's a hands-on position offering impact in a regulated environment with hybrid working and a clear regulatory focus.
Senior Verification & Validation Engineer (V&V) – Embedded Software | DO-178C | Safety Critical SystemsAre you an experienced Verification & Validation Engineer, Software Test Engineer, or Systems Verification Engineer with a background in safety-critical embedded software?We're recruiting for an exciting...
£75,000 - £80,000 per annum + 20% Bonus + Car AllowanceOffice is based in Hampshire, close to the Surrey borderFull Time | PermanentRegular UK Travel requiredOur client is an established international manufacturing and engineering business supplying innovative material solutions to...
The Global Labelling Director, Content will lead the development and delivery of high-quality global labelling strategies for innovative medicines. Key responsibilities include shaping labelling content, maintaining core documents, and collaborating with cross-functional teams to ensure regulatory compliance and successful product submissions.
The Senior Regulatory Associate at Pfizer is responsible for managing regulatory activities for assigned products and markets, including new registrations, MA variations, and renewals. They will work closely with cross-functional teams, national regulatory authorities, and above-country hubs to ensure compliance and support clinical development activities.
Head of MarketingLocation: West SussexSalary: Up to £70,000, Plus BenefitsDrive the marketing function for a respected manufacturer supplying global organisations. This is a hands‑on Head of Marketing role ideal for a commercially minded marketer who enjoys both strategy and execution.About...
Job Title: Senior Embedded Software EngineerLocation: Newcastle-Upon-Tyne, Hybrid (3/2)Salary: £60-70K + bonusWe're looking for an experienced Senior Embedded Software Engineer to lead firmware development and drive delivery of embedded products. You'll manage key projects, mentor engineers, and work closely with...
